Methods of preparing lipid nanoparticles

Abstract

The present disclosure provides methods of preparing lipid nanoparticle (LNP) formulations. The present disclosure also provides therapeutic and diagnostic uses related to the prepared LNP formulations.

Description

METHODS OF PREPARING LIPID NANOPARTICLESRELATED APPLICATIONS

[0001] This application claims priority to, and the benefit of, U.S. Application No. 63 / 625,708, filed January 26, 2024, which is hereby incorporated by reference in its entirety.BACKGROUND

[0002] The effective targeted delivery of biologically active substances such as small molecule drugs, proteins, and nucleic acids represents a continuing medical challenge. In particular, the delivery of nucleic acids to cells is made difficult by the relative instability and low cell permeability of such species. Thus, there exists a need to develop methods and compositions to facilitate the delivery of therapeutics and prophylactics such as nucleic acids to cells.

[0003] Lipid-containing nanoparticles or lipid nanoparticles, liposomes, and lipoplexes have proven effective as transport vehicles into cells and / or intracellular compartments for biologically active substances such as small molecule drugs, proteins, and nucleic acids. Though a variety of such lipid-containing nanoparticles have been demonstrated, improvements in safety, efficacy, and specificity are still lacking.SUMMARY

[0004] In some aspects, the present disclosure provides methods of preparing an empty-lipid nanoparticle solution (empty-LNP solution) comprising an empty lipid nanoparticle (empty LNP), wherein the method comprises: i) a nanoprecipitation step, comprising: i-a) a mixing step, comprising mixing a lipid solution comprising an ionizable lipid, a structural lipid, and a phospholipid, with a first aqueous buffer solution, thereby forming an intermediate empty-lipid nanoparticle solution (intermediate empty-LNP solution) comprising an intermediate empty lipid nanoparticle (intermediate empty LNP); i-b) a holding step, comprising holding the intermediate empty-LNP solution for a residence time; and i-c) a diluting step, comprising adding a diluting solution comprising a second aqueous buffer solution to the intermediate empty-LNP solution, thereby forming the empty-LNP solution comprising an empty LNP,wherein the lipid solution, the aqueous buffer solution, and / or the diluting solution comprises a phosphatidylserine phospholipid.

[0005] In some aspects, the present disclosure provides an empty -LNP solution comprising the population of empty LNPs disclosed herein.

[0006] In some aspects, the present disclosure provides an empty-LNP formulation comprising the population of empty LNPs disclosed herein.

[0007] In some aspects, the present disclosure provides a loaded-LNP solution comprising a loaded LNP disclosed herein.

[0008] In some aspects, the present disclosure provides a loaded-LNP formulation comprising a loaded LNP disclosed herein.

[0009] In some aspects, the present disclosure provides a method of treating or preventing a disease or disorder, the method comprising administering to a subject in need thereof the loaded-LNP solution disclosed herein.

[0010] In some aspects, the present disclosure provides a method of treating or preventing a disease or disorder, the method comprising administering to a subject in need thereof the loaded-LNP formulation disclosed herein.

[0011] In some aspects, the present disclosure provides a loaded-LNP solution disclosed herein for use in treating or preventing a disease or disorder in a subject.

[0012] In some aspects, the present disclosure provides a loaded-LNP formulation disclosed herein for use in treating or preventing a disease or disorder in a subject.

[0013] In some aspects, the present disclosure provides use of the loaded-LNP solution disclosed herein in the manufacture of a medicament for treating or preventing a disease or disorder.

[0014] In some aspects, the present disclosure provides use of the loaded-LNP formulation disclosed herein in the manufacture of a medicament for treating or preventing a disease or disorder.

[0015] In some aspects, the present disclosure provides a pharmaceutical kit, comprising an empty LNP described herein, an empty-LNP solution described herein, an empty-LNP formulation described herein, a loaded LNP described herein, a loaded-LNP solution, or a loaded LNP formulation described herein.

[0016] Unless otherwise defined, all technical and scientific terms used herein have the same meaning as commonly understood by one of ordinary skill in the art to which this disclosure belongs. Although methods and materials similar or equivalent to those described herein can be used in the practice or testing of the present disclosure, suitable methods and materials aredescribed below. All publications, patent applications, patents, and other references mentioned herein are incorporated by reference in their entirety. In the case of conflict, the present specification, including definitions, will control. In addition, the materials, methods, and examples are illustrative only and are not intended to be limiting.

[0017] Other features and advantages of the disclosure will be apparent from the following detailed description and claims.BRIEF DESCRIPTION OF THE DRAWINGS

[0018] FIG. 1 is a process flow diagram for manufacturing DMPS empty nanoparticle (empty LNP).

[0019] FIG. 2 is a set of graphs showing representative zeta potential distribution of (A) IL- 6 / DMPS empty LNP, (B) IL-8 / DMPS empty LNP, and (C) IL-l / DMPS empty LNP manufactured by the #2 process.

[0020] FIG. 3A is a SAXS gragh for IL-8 / DMPS empty LNP produced via the #1 process but exchanged into different storage buffers (phosphate buffer with different pHs and acetate buffer).

[0021] FIG. 3B is a graph that shows zeta potential traces for IL-8 / DMPS empty LNP produced via the #1 process but exchanged into different storage buffers (phosphate buffer with different pHs and acetate buffer).

[0022] FIG. 4A is a graph showing in process SAXS profiles for IL-6 / DMPS #2 process empty LNP post in-line dilution, buffer exchange into acetate and sucrose.

[0023] FIG. 4B is a graph showing in process SAXS profiles for IL-8 / DMPS #2 process empty LNP post in-line dilution, buffer exchange into acetate and sucrose.

[0024] FIG. 4C is a graph showing in process SAXS profiles for IL-l / DMPS #2 process empty LNP post in-line dilution, buffer exchange into acetate and sucrose.DETAILED DESCRIPTIONMethods of the Present Disclosure

[0025] In some aspects, the present disclosure provides a method of preparing an empty-lipid nanoparticle solution (empty-LNP solution), comprising: i) a nanoprecipitation step, comprising: i-a) a mixing step, comprising mixing a lipid solution comprising an ionizable lipid, a structural lipid, and a phospholipid, with a first aqueous buffer solution, thereby forming an intermediate empty-lipid nanoparticle solution (intermediate empty-LNPsolution) comprising an intermediate empty lipid nanoparticle (intermediate empty LNP); i-b) a holding step, comprising holding the intermediate empty-LNP solution for a residence time; and i-c) a diluting step, comprising adding a diluting solution comprising a second aqueous buffer solution to the intermediate empty-LNP solution, thereby forming the empty-LNP solution comprising an empty LNP, wherein the lipid solution, the aqueous buffer solution, and / or the diluting solution comprises a phosphatidylserine phospholipid.

[0026] In some aspects, the present disclosure provides a method of preparing an empty -lipid nanoparticle formulation (empty-LNP formulation), comprising: i) a nanoprecipitation step, comprising: i-a) a mixing step, comprising mixing a lipid solution comprising an ionizable lipid, a structural lipid, and a phospholipid, with a first aqueous buffer solution, thereby forming an intermediate empty-lipid nanoparticle solution (intermediate empty-LNP solution) comprising an intermediate empty lipid nanoparticle (intermediate empty LNP); i-b) a holding step, comprising holding the intermediate empty-LNP solution for a residence time; and i-c) a diluting step, comprising adding a diluting solution comprising a second aqueous buffer solution to the intermediate empty-LNP solution, thereby forming the empty-LNP solution comprising an empty LNP, and ii) processing the empty-LNP solution, thereby forming an empty-LNP formulation, wherein the lipid solution, the aqueous buffer solution, and / or the diluting solution comprises a phosphatidylserine phospholipid.

[0027] In some aspects, the present disclosure provides a method of preparing a loaded lipid nanoparticle solution (loaded-LNP solution), comprising: i) a nanoprecipitation step, comprising: i-a) a mixing step, comprising mixing a lipid solution comprising an ionizable lipid, a structural lipid, and a phospholipid, with a first aqueous buffer solution, thereby forming an intermediate empty-lipid nanoparticle solution (intermediate empty-LNP solution) comprising an intermediate empty lipid nanoparticle (intermediate empty LNP);i-b) a holding step, comprising holding the intermediate empty-LNP solution for a residence time; and i-c) a diluting step, comprising adding a diluting solution comprising a second aqueous buffer solution to the intermediate empty-LNP solution, thereby forming the empty-LNP solution comprising an empty LNP, iii) mixing a nucleic acid solution comprising a nucleic acid with the empty-LNP solution, thereby forming the loaded-LNP solution comprising a loaded lipid nanoparticle (loaded LNP), wherein the lipid solution, the aqueous buffer solution, and / or the diluting solution comprises a phosphatidylserine phospholipid.

[0028] In some aspects, the present disclosure provides a method of preparing a loaded lipid nanoparticle solution (loaded-LNP solution), comprising: i) a nanoprecipitation step, comprising: i-a) a mixing step, comprising mixing a lipid solution comprising an ionizable lipid, a structural lipid, and a phospholipid, with a first aqueous buffer solution, thereby forming an intermediate empty-lipid nanoparticle solution (intermediate empty-LNP solution) comprising an intermediate empty lipid nanoparticle (intermediate empty LNP); i-b) a holding step, comprising holding the intermediate empty-LNP solution for a residence time; and i-c) a diluting step, comprising adding a diluting solution comprising a second aqueous buffer solution to the intermediate empty-LNP solution, thereby forming the empty-LNP solution comprising an empty LNP, ii) processing the empty-LNP solution, thereby forming an empty-LNP formulation; and iii) mixing a nucleic acid solution comprising a nucleic acid with the empty-LNP formulation, thereby forming the loaded-LNP solution comprising a loaded lipid nanoparticle (loaded LNP), wherein the lipid solution, the aqueous buffer solution, and / or the diluting solution comprises a phosphatidylserine phospholipid.

[0029] In some aspects, the present disclosure provides a method of preparing a loaded lipid nanoparticle formulation (loaded-LNP formulation), comprising: i) a nanoprecipitation step, comprising:i-a) a mixing step, comprising mixing a lipid solution comprising an ionizable lipid, a structural lipid, and a phospholipid, with a first aqueous buffer solution, thereby forming an intermediate empty-lipid nanoparticle solution (intermediate empty-LNP solution) comprising an intermediate empty lipid nanoparticle (intermediate empty LNP); i-b) a holding step, comprising holding the intermediate empty-LNP solution for a residence time; and i-c) a diluting step, comprising adding a diluting solution comprising a second aqueous buffer solution to the intermediate empty-LNP solution, thereby forming the empty-LNP solution comprising an empty LNP, iii) mixing a nucleic acid solution comprising a nucleic acid with the empty-LNP solution, thereby forming the loaded-LNP solution comprising a loaded lipid nanoparticle (loaded LNP); and iv) processing the loaded-LNP solution, thereby forming a loaded-LNP formulation, wherein the lipid solution, the aqueous buffer solution, and / or the diluting solution comprises a phosphatidylserine phospholipid.

[0030] In some aspects, the present disclosure provides a method of preparing a loaded lipid nanoparticle formulation (loaded-LNP formulation), comprising: i) a nanoprecipitation step, comprising: i-a) a mixing step, comprising mixing a lipid solution comprising an ionizable lipid, a structural lipid, and a phospholipid, with a first aqueous buffer solution, thereby forming an intermediate empty-lipid nanoparticle solution (intermediate empty-LNP solution) comprising an intermediate empty lipid nanoparticle (intermediate empty LNP); i-b) a holding step, comprising holding the intermediate empty-LNP solution for a residence time; and i-c) a diluting step, comprising adding a diluting solution comprising a second aqueous buffer solution to the intermediate empty-LNP solution, thereby forming the empty-LNP solution comprising an empty LNP, ii) processing the empty-LNP solution, thereby forming an empty-LNP formulation; iii) mixing a nucleic acid solution comprising a nucleic acid with the empty-LNP formulation, thereby forming the loaded-LNP solution comprising a loaded lipid nanoparticle (loaded LNP); and iv) processing the loaded-LNP solution, thereby forming a loaded-LNP formulation,wherein the lipid solution, the aqueous buffer solution, and / or the diluting solution comprises a phosphatidylserine phospholipid.

[0031] In some embodiments, the lipid solution comprises the phosphatidylserine phospholipid.

[0032] In some embodiments, the aqueous buffer solution comprises the phosphatidylserine phospholipid.

[0033] In some embodiments, the diluting solution comprises the phosphatidylserine phospholipid.

[0034] In some embodiments, the empty LNP comprises the phosphatidylserine phospholipid.Mixing Step

[0035] In some embodiments, the methods of the present disclosure comprise i) a nanoprecipitation step, comprising i-a) mixing step, comprising mixing a lipid solution comprising an ionizable lipid, a structural lipid, a phospholipid, and a PEG lipid, with an aqueous buffer solution comprising a first buffering agent, thereby forming an intermediate empty-lipid nanoparticle solution (intermediate empty-LNP solution) comprising an intermediate empty nanoparticle (intermediate empty LNP).

[0036] In some embodiments, the mixing step is performed with a first aqueous buffer solution having a pH higher than the pKa of the ionizable lipid.

[0037] In some embodiments, the mixing step is performed at a pH of 12.0±2.0, 12.0±1.5, 12.0±1.0, 12.0±0.9, 12.0±0.8, 12.0±0.7, 12.0±0.6, 12.0±0.5, 12.0±0.4, 12.0±0.3, 12.0±0.2, or 12.0±0.1.

[0038] In some embodiments, the mixing step is performed with a first aqueous buffer solution having a pH of about 12.0. In some embodiments, the mixing step is performed with a first aqueous buffer solution compring phosphate buffer. In some embodiments, the mixing step is performed with a first aqueous buffer solution comprising phosphate buffer at about pH 12.0.

[0039] In some embodiments, the mixing step is performed with a lipid solution further comprising from about 0.1 mol% to about 0.5 mol% PEG lipid, a phospholipid, a structural lipid, or any combination thereof.

[0040] In some embodiments, the mixing step is performed with a lipid solution comprising about 30-60 mol% ionizable lipid; about 0-30 mol% phospholipid; about 15-50 mol% structural lipid; and about 0.1-0.5 mol% PEG lipid.

[0041] In some embodiments, the mixing step is performed with a lipid solution comprising about 30-60 mol% ionizable lipid; about 0-30 mol% phospholipid; about 15-50 mol% structural lipid; and about 0.1-10 mol% PEG lipid.

[0042] In some embodiments, the mixing step is performed with a lipid solution comprising IL-2, DSPC, SL-2, and PEG2k-DMG.

[0043] In some embodiments, the mixing step is performed with a lipid solution comprising about 30-60 mol% IL-2; about 0-30 mol% DSPC; about 15-50 mol% SL-2; and about 0.1-0.5 mol% PEG2k-DMG. In some embodiments, the mixing step is performed with a lipid solution comprising about 0-30 mol% DSPC; about 15-50 mol% SL-2; and about 0.1-0.5 mol% PEG2k- DMG. In some embodiments, the mixing step is performed with a lipid solution comprising about 30-60 mol% IL-2; about 15-50 mol% SL-2; and about 0.1-0.5 mol% PEG2k-DMG. In some embodiments, the mixing step is performed with a lipid solution comprising about 30-60 mol% IL-2; about 0-30 mol% DSPC; and about 0.1-0.5 mol% PEG2k-DMG. In some embodiments, the mixing step is performed with a lipid solution comprising about 30-60 mol% IL-2; about 0-30 mol% DSPC; and about 15-50 mol% SL-2. In some embodiments, the mixing step is performed with a lipid solution comprising about 30-60 mol% IL-2 and about 0.1-0.5 mol% PEG2k-DMG. In some embodiments, the mixing step is performed with a lipid solution comprising about 30-60 mol% IL-2 and about 0-30 mol% DSPC. In some embodiments, the mixing step is performed with a lipid solution comprising about 30-60 mol% IL-2 and about 15-50 mol% SL-2. In some embodiments, the mixing step is performed with a lipid solution comprising about 0-30 mol% DSPC and about 15-50 mol% SL-2. In some embodiments, the mixing step is performed with a lipid solution comprising about 0-30 mol% DSPC and about 0.1-0.5 mol% PEG2k-DMG. In some embodiments, the mixing step is performed with a lipid solution comprising about about 15-50 mol% SL-2 and about 0.1-0.5 mol% PEG2k-DMG. In some embodiments, the mixing step is performed with a lipid solution comprising about 30-60 mol% IL-2. In some embodiments, the mixing step is performed with a lipid solution comprising about 0-30 mol% DSPC. In some embodiments, the mixing step is performed with a lipid solution comprising about 15-50 mol% SL-2. In some embodiments, the mixing step is performed with a lipid solution comprising about 0.1-0.5 mol% PEG2k-DMG.

[0044] In some embodiments, the mixing step is performed with a lipid solution comprising about 30-60 mol% IL-2; about 0-30 mol% DSPC; about 15-50 mol% SL-2; and about 0.1-10 mol% PEG2k-DMG. In some embodiments, the mixing step is performed with a lipid solution comprising about 0-30 mol% DSPC; about 15-50 mol% SL-2; and about 0.1-10 mol% PEG2k- DMG. In some embodiments, the mixing step is performed with a lipid solution comprisingabout 0-30 mol% DSPC; about 15-50 mol% SL-2; and about 0.1-10 mol% PEG2k-DMG. In some embodiments, the mixing step is performed with a lipid solution comprising about 30-60 mol% IL-2; about 15-50 mol% SL-2; and about 0.1-10 mol% PEG2k-DMG. In some embodiments, the mixing step is performed with a lipid solution comprising about 30-60 mol% IL-2; about 0-30 mol% DSPC; and about 0.1-10 mol% PEG2k-DMG. In some embodiments, the mixing step is performed with a lipid solution comprising about 30-60 mol% IL-2; about 0-30 mol% DSPC; and about 15-50 mol% SL-2. In some embodiments, the mixing step is performed with a lipid solution comprising about 30-60 mol% IL-2 and about 0-30 mol% DSPC. In some embodiments, the mixing step is performed with a lipid solution comprising about 30-60 mol% IL-2 and about 15-50 mol% SL-2. In some embodiments, the mixing step is performed with a lipid solution comprising about 30-60 mol% IL-2 and about 0.1-10 mol% PEG2k-DMG. In some embodiments, the mixing step is performed with a lipid solution comprising about 0-30 mol% DSPC and about 15-50 mol% SL-2. In some embodiments, the mixing step is performed with a lipid solution comprising about 0-30 mol% DSPC about 0.1- 10 mol% PEG2k-DMG. In some embodiments, the mixing step is performed with a lipid solution comprising about 15-50 mol% SL-2 and about 0.1-10 mol% PEG2k-DMG. In some embodiments, the mixing step is performed with a lipid solution comprising about 30-60 mol% IL-2. In some embodiments, the mixing step is performed with a lipid solution comprising about 0-30 mol% DSPC. In some embodiments, the mixing step is performed with a lipid solution comprising about 15-50 mol% SL-2. In some embodiments, the mixing step is performed with a lipid solution comprising about 0.1-10 mol% PEG2k-DMG.

[0045] In some embodiments, the mixing step is performed with a lipid solution comprising from about 20 to about 70 mg / mL ionizable lipid, about 25 to about 65 mg / mL ionizable lipid, about 30 to about 60 mg / mL ionizable lipid, about 35 to about 55 mg / mL ionizable lipid, about 40 to about 50 mg / mL ionizable lipid, or about 45 to about 50 mg / mL ionizable lipid.

[0046] In some embodiments, the mixing step is performed with a lipid solution comprising from about 5.0 to about 20 mg / mL ionizable lipid, about 7.5 to about 17.5 mg / mL ionizable lipid, about 10 to about 15 mg / mL ionizable lipid, or about 12.5 to about 15 mg / mL ionizable lipid.

[0047] In some embodiments, the mixing step is performed with a lipid solution comprising about 20 mg / mL ionizable lipid, about 25 mg / mL ionizable lipid, about 30 mg / mL ionizable lipid, about 35 mg / mL ionizable lipid, about 40 mg / mL ionizable lipid, about 45 mg / mL ionizable lipid, about 50 mg / mL ionizable lipid, about 55 mg / mL ionizable lipid, about 60 mg / mL ionizable lipid, about 65 mg / mL ionizable lipid, or about 70 mg / mL ionizable lipid.

[0048] In some embodiments, the mixing step is performed with a lipid solution comprising about 5.0 mg / mL ionizable lipid, about 7.5 mg / mL ionizable lipid, about 10 mg / mL ionizable lipid, about 12.5 mg / mL ionizable lipid, about 15 mg / mL ionizable lipid, about 17.5 mg / mL ionizable lipid, or about 20 mg / mL ionizable lipid.

[0049] In some embodiments, the mixing step is performed with a lipid solution comprising from about 5 to about 35 mg / mL structural lipid, about 10 to about 30 mg / mL structural lipid, about 15 to about 25 mg / mL structural lipid, or about 20 to about 25 mg / mL structural lipid.

[0050] In some embodiments, the mixing step is performed with a lipid solution comprising from about 1.0 to about 8.0 mg / mL structural lipid, about 2.0 to about 7.0 mg / mL structural lipid, about 3.0 to about 6.0 mg / mL structural lipid, or about 4.0 to about 5.0 mg / mL structural lipid.

[0051] In some embodiments, the mixing step is performed with a lipid solution comprising about 5 mg / mL structural lipid, about 10 mg / mL structural lipid, about 15 mg / mL structural lipid, about 20 mg / mL structural lipid, about 25 mg / mL structural lipid, about 30 mg / mL structural lipid, about 35 mg / mL structural lipid, or about 40 mg / mL structural lipid.

[0052] In some embodiments, the mixing step is performed with a lipid solution comprising about 1.0 mg / mL structural lipid, about 2.0 mg / mL structural lipid, about 3.0 mg / mL structural lipid, about 4.0 mg / mL structural lipid, about 5.0 mg / mL structural lipid, about 6.0 mg / mL structural lipid, about 7.0 mg / mL structural lipid, or about 8.0 mg / mL structural lipid.

[0053] In some embodiments, the mixing step is performed with a lipid solution comprising from about 2.5 to about 20 mg / mL phospholipid, about 5 to about 17.5 mg / mL phospholipid, about 7.5 to about 15 mg / mL phospholipid, or about 10 to about 12.5 mg / mL phospholipid.

[0054] In some embodiments, the mixing step is performed with a lipid solution comprising from about 1.0 to about 5.0 mg / mL phospholipid, about 1.5 to about 4.5 mg / mL phospholipid, about 2.0 to about 4.0 mg / mL phospholipid, about 2.5 to about 3.5 mg / mL phospholipid or about 3.0 mg / mL to about 3.5 mg / mL.

[0055] In some embodiments, the mixing step is performed with a lipid solution comprising about 2.5 mg / mL phospholipid, about 5 mg / mL phospholipid, about 7.5 mg / mL phospholipid, about 10 mg / mL phospholipid, about 12.5 mg / mL phospholipid, about 15 mg / mL phospholipid, about 17.5 mg / mL phospholipid, or about 20 mg / mL phospholipid.

[0056] In some embodiments, the mixing step is performed with a lipid solution comprising about 1.0 mg / mL phospholipid, about 1.5 mg / mL phospholipid, about 2.0 mg / mL phospholipid, about 2.5 mg / mL phospholipid, about 3.0 mg / mL phospholipid, about 3.5 mg / mL phospholipid, about 4.5 mg / mL phospholipid, or about 5.0 mg / mL phospholipid.

[0057] In some embodiments, the mixing step is performed with a lipid solution comprising from about 0.05 to about 5.5 mg / mL PEG lipid, about 0.1 to about 5.0 mg / mL PEG lipid, about 0.25 to about 4.5 mg / mL PEG lipid, about 0.5 to about 4.0 mg / mL PEG lipid, about 1.0 to about 3.5 mg / mL PEG lipid, about 1.5 to about 3.0 mg / mL PEG lipid, or about 2.0 to about 2.5 mg / mL PEG lipid.

[0058] In some embodiments, the mixing step is performed with a lipid solution comprising from about 0.05 mg / mL PEG lipid, about 0.1 mg / mL PEG lipid, about 0.25 mg / mL PEG lipid, about 0.5 mg / mL PEG lipid, about 1.0 mg / mL PEG lipid, about 1.5 mg / mL PEG lipid, about 2.5 mg / mL PEG lipid, about 3.0 mg / mL PEG lipid, about 3.5 mg / mL PEG lipid, about 4.0 mg / mL PEG lipid, about 4.5 mg / mL PEG lipid, or about 5.0 mg / mL PEG lipid.

[0059] In some embodiments, the mixing step is performed with a lipid solution comprising from about 10 to about 20 mg / mL ionizable lipid; about 2.0 to about 8.0 mg / mL structural lipid; about 1.0 to about 5.0 phospholipid; and from about 0.1 to about 5.0 mg / mL PEG lipid.

[0060] In some embodiments, the mixing step is performed with a total lipid concentration from about 5 mg / mL to about 80 mg / mL, about 6 mg / mL to about 70 mg / mL, about 7 mg / mL to about 60 mg / mL, about 8 mg / mL to about 50 mg / mL, about 9 mg / mL to about 40 mg / mL, about 10 mg / mL to about 30 mg / mL, about 15 mg / mL to about 25 mg / mL, or about 20 mg / mL to about 25 mg / mL.

[0061] In some embodiments, the mixing step is performed with a total lipid concentration of about 10 mg / mL, about 15 mg / mL, about 20 mg / mL, about 25 mg / mL, about 30 mg / mL, about 40 mg / mL, about 50 mg / mL, about 60 mg / mL, about 70 mg / mL, or about 80 mg / mL.

[0062] In some embodiments, the mixing step is performed with a lipid solution comprising from about 30 mg / mL to about 60 mg / mL ionizable lipid; about 10 mg / mL to about 30 mg / mL structural lipid; about 5 mg / mL to about 15 mg / mL phospholipid; and from about 0.1 mg / mL to about 5.0 mg / mL PEG lipid.

[0063] In some embodiments, the mixing step is performed with a lipid solution comprising from about 30 mg / mL to about 60 mg / mL IL-1; about 10 to about 30 mg / mL SL-2; about 5 mg / mL to about 15 mg / mL DSPC; and from about 0.1 mg / mL to about 5.0 mg / mL PEG2k- DMG.

[0064] In some embodiments, the mixing step is performed with a lipid solution comprising from about 30 mg / mL to about 60 mg / mL IL-2; about 10 to about 30 mg / mL SL-2; about 5 mg / mL to about 15 mg / mL DSPC; and from about 0.1 mg / mL to about 5.0 mg / mL PEG2k- DMG.

[0065] In some embodiments, the mixing step is performed with a lipid solution comprising from about 10 mg / mL to about 20 mg / mL ionizable lipid; about 4 mg / mL to about 8 mg / mL structural lipid; about 2 mg / mL to about 5 mg / mL phospholipid; and from about 0.1 mg / mL to about 1.0 mg / mL PEG lipid.

[0066] In some embodiments, the mixing step is performed with a lipid solution comprising from about 10 mg / mL to about 20 mg / mL IL-1; about 4 mg / mL to about 8 mg / mL SL-2; about 2 mg / mL to about 5 mg / mL DSPC; and from about 0.1 mg / mL to about 1.0 mg / mL PEG2k- DMG.

[0067] In some embodiments, the mixing step is performed with a lipid solution comprising from about 10 mg / mL to about 20 mg / mL IL-2; about 4 mg / mL to about 8 mg / mL SL-2; about 2 mg / mL to about 5 mg / mL DSPC; and from about 0.1 mg / mL to about 1.0 mg / mL PEG2k- DMG.

[0068] In some embodiments, the mixing step is performed with a T-junction, confined impinging jets, microfluidic mixer, or vortex mixer.

[0069] In some embodiments, the mixing step is performed with a barbed tee.

[0070] In some embodiments, the mixing step is performed with a flow rate of about 1 mL / min to about 300 mL / min, about 5 mL / min to about 250 mL / min, about 10 mL / min to about 200 mL / min, about 25 mL / min to about 175 mL / min, about 50 mL / min to about 150 mL / min, about 75 mL / min to about 125 mL / min, or about 100 mL / min to about 125 mL / min.

[0071] In some embodiments, the mixing step is performed with a flow rate of about 1 mL / min, about 5 mL / min, about 10 mL / min, about 25 mL / min, about 50 mL / min, about 75 mL / min, about 100 mL / min, about 125 mL / min, about 150 mL / min, about 175 mL / min, about 200 mL / min, about 250 mL / min, or about 300 mL / min.

[0072] In some embodiments, the mixing step is performed with a lipid solution flow rate of about 1 mL / min, about 5 mL / min, about 10 mL / min, about 25 mL / min, about 50 mL / min, about 75 mL / min, about 100 mL / min, about 125 mL / min, about 150 mL / min, about 175 mL / min, about 200 mL / min, about 250 mL / min, or about 300 mL / min.

[0073] In some embodiments, the mixing step is performed with a lipid solution flow rate of about 1 mL / min, about 5 mL / min, about 10 mL / min, about 25 mL / min, about 50 mL / min, about 75 mL / min, about 100 mL / min, about 125 mL / min, about 150 mL / min, about 175 mL / min, about 200 mL / min, about 250 mL / min, or about 300 mL / min.

[0074] In some embodiments, the mixing step is performed with a nucleic acid solution flow rate of about 1 mL / min, about 5 mL / min, about 10 mL / min, about 25 mL / min, about 50mL / min, about 75 mL / min, about 100 mL / min, about 125 mL / min, about 150 mL / min, about 175 mL / min, about 200 mL / min, about 250 mL / min, or about 300 mL / min.

[0075] In some embodiments, the mixing step is performed with an aqueous buffer flow rate of about 1 mL / min, about 5 mL / min, about 10 mL / min, about 25 mL / min, about 50 mL / min, about 75 mL / min, about 100 mL / min, about 125 mL / min, about 150 mL / min, about 175 mL / min, about 200 mL / min, about 250 mL / min, or about 300 mL / min.

[0076] In some embodiments, the mixing step is performed with an aqueous buffer flow rate of about 1 mL / min, about 5 mL / min, about 10 mL / min, about 25 mL / min, about 50 mL / min, about 75 mL / min, about 100 mL / min, about 125 mL / min, about 150 mL / min, about 175 mL / min, about 200 mL / min, about 250 mL / min, or about 300 mL / min.

[0077] In some embodiments, the mixing step is performed with an aqueous buffer flow rate of about 1 mL / min, about 5 mL / min, about 10 mL / min, about 25 mL / min, about 50 mL / min, about 75 mL / min, about 100 mL / min, about 125 mL / min, about 150 mL / min, about 175 mL / min, about 200 mL / min, about 250 mL / min, or about 300 mL / min.

[0078] In some embodiments, the mixing step is performed with a first aqueous buffer flow rate of about 1 mL / min, about 5 mL / min, about 10 mL / min, about 25 mL / min, about 50 mL / min, about 75 mL / min, about 100 mL / min, about 125 mL / min, about 150 mL / min, about 175 mL / min, about 200 mL / min, about 250 mL / min, or about 300 mL / min.

[0079] In some embodiments, the mixing step is performed with a first aqueous buffer flow rate of about 1 mL / min, about 5 mL / min, about 10 mL / min, about 25 mL / min, about 50 mL / min, about 75 mL / min, about 100 mL / min, about 125 mL / min, about 150 mL / min, about 175 mL / min, about 200 mL / min, about 250 mL / min, or about 300 mL / min.

[0080] In some embodiments, the mixing step is performed with a second aqueous buffer flow rate of about 1 mL / min, about 5 mL / min, about 10 mL / min, about 25 mL / min, about 50 mL / min, about 75 mL / min, about 100 mL / min, about 125 mL / min, about 150 mL / min, about 175 mL / min, about 200 mL / min, about 250 mL / min, or about 300 mL / min.

[0081] In some embodiments, the mixing step is performed with a second aqueous buffer flow rate of about 1 mL / min, about 5 mL / min, about 10 mL / min, about 25 mL / min, about 50 mL / min, about 75 mL / min, about 100 mL / min, about 125 mL / min, about 150 mL / min, about 175 mL / min, about 200 mL / min, about 250 mL / min, or about 300 mL / min.

[0082] In some embodiments, the mixing step is performed with a third aqueous buffer flow rate of about 1 mL / min, about 5 mL / min, about 10 mL / min, about 25 mL / min, about 50 mL / min, about 75 mL / min, about 100 mL / min, about 125 mL / min, about 150 mL / min, about 175 mL / min, about 200 mL / min, about 250 mL / min, or about 300 mL / min.

[0083] In some embodiments, the mixing step is performed with a third aqueous buffer flow rate of about 1 mL / min, about 5 mL / min, about 10 mL / min, about 25 mL / min, about 50 mL / min, about 75 mL / min, about 100 mL / min, about 125 mL / min, about 150 mL / min, about 175 mL / min, about 200 mL / min, about 250 mL / min, or about 300 mL / min.

[0084] In some embodiments, the mixing step is performed at a temperature of less than about 50 °C, less than about 45 °C, less than about 50 °C, less than about 35 °C, less than about 30 °C, less than about 28 °C, less than about 26 °C, less than about 24 °C, less than about 22 °C, less than about 20 °C, or less than about ambient temperature.

[0085] In some embodiments, the mixing step is performed at a temperature of about 50 °C, about 45 °C, about 50 °C, about 35 °C, about 30 °C, about 28 °C, about 26 °C, about 24 °C, about 22 °C, about 20 °C, or about ambient temperature.Lipid Solutions

[0086] In some embodiments, the methods of the present disclosure provide a lipid solution comprising an ionizable lipid, a structural lipid, a phospholipid, and a PEG lipid.

[0087] In some embodiments, the lipid solution comprises a phosphatidylserine phospholipid.

[0088] In some embodiments, the lipid solution further comprises an encapsulation agent.

[0089] In some embodiments, the ionizable lipid is present in the lipid solution at a concentration of greater than about 0.01 mg / mL, 0.05 mg / mL, 0.06 mg / mL, 0.07 mg / mL, 0.08 mg / mL, 0.09 mg / mL, 0.1 mg / mL, 0.15 mg / mL, 0.2 mg / mL, 0.3 mg / mL, 0.4 mg / mL, 0.5 mg / mL, 0.6 mg / mL, 0.7 mg / mL, 0.8 mg / mL, 0.9 mg / mL, or 1.0 mg / mL.

[0090] In some embodiments, the ionizable lipid is present in the lipid solution at a concentration ranging from about 0.01-1.0 mg / mL, 0.01-0.9 mg / mL, 0.01-0.8 mg / mL, 0.01- 0.7 mg / mL, 0.01-0.6 mg / mL, 0.01-0.5 mg / mL, 0.01-0.4 mg / mL, 0.01-0.3 mg / mL, 0.01-0.2 mg / mL, 0.01-0.1 mg / mL, 0.05-1.0 mg / mL, 0.05-0.9 mg / mL, 0.05-0.8 mg / mL, 0.05-0.7 mg / mL, 0.05-0.6 mg / mL, 0.05-0.5 mg / mL, 0.05-0.4 mg / mL, 0.05-0.3 mg / mL, 0.05-0.2 mg / mL, 0.05-0.1 mg / mL, 0.1-1.0 mg / mL, 0.2-0.9 mg / mL, 0.3-0.8 mg / mL, 0.4-0.7 mg / mL, or 0.5-0.6 mg / mL.

[0091] In some embodiments, the ionizable lipid is present in the lipid solution at a concentration up to about 5.0 mg / mL, 4.0 mg / mL, 3.0 mg / mL, 2.0 mg / mL, 1.0 mg / mL, 0.09 mg / mL, 0.08 mg / mL, 0.07 mg / mL, 0.06 mg / mL, or 0.05 mg / mL.

[0092] In some embodiments, the ionizable lipid is present in the lipid solution at a concentration of greater than about 0.1 mg / mL, 0.5 mg / mL, 0.6 mg / mL, 0.7 mg / mL, 0.8 mg / mL, 0.9 mg / mL, 1.0 mg / mL, 1.5 mg / mL, 2.0 mg / mL, 3.0 mg / mL, 4.0 mg / mL, 5.0 mg / mL,6.0 mg / mL, 7.0 mg / mL, 8.0 mg / mL, 9.0 mg / mL, 10 mg / mL, 11 mg / mL, 12 mg / mL, 13 mg / mL, 14 mg / mL, 15 mg / mL, 20 mg / mL, 25 mg / mL or 30 mg / mL. In some embodiments, the lipid solution comprises a ionizable lipid at a concentration ranging from about 0.1-20.0 mg / mL, 0.1-19 mg / mL, 0.1-18 mg / mL, 0.1-17 mg / mL, 0.1-16 mg / mL, 0.1-15 mg / mL, 0.1-14 mg / mL, 01-13 mg / mL, 0.1-12 mg / mL, 0.1-11 mg / mL, 0.5-10.0 mg / mL, 0.5-9 mg / mL, 0.5-8 mg / mL, 0.5-7 mg / mL, 0.5-6 mg / mL, 0.5-5.0 mg / mL, 0.5-4 mg / mL, 0.5-3 mg / mL, 0.5-2 mg / mL, 0.5-1 mg / mL, 1-20 mg / mL, 1-15 mg / mL, 1-12 mg / mL, 1-10 mg / mL, or 1-8 mg / mL. In some embodiments, the lipid solution comprises an ionizable lipid at a concentration up to about 30 mg / mL, 25, mg / mL, 20 mg / mL, 18 mg / mL, 16 mg / mL, 15 mg / mL, 14 mg / mL, 12 mg / mL, 10 mg / mL, 8 mg / mL, 6 mg / mL, 5.0 mg / mL, 4.0 mg / mL, 3.0 mg / mL, 2.0 mg / mL, 1.0 mg / mL, 0.09 mg / mL, 0.08 mg / mL, 0.07 mg / mL, 0.06 mg / mL, or 0.05 mg / mL.

[0093] In some embodiments, the ionizable lipid is present in the lipid solution at a concentration of about 30 mol % to about 70 mol %.

[0094] In some embodiments, the structural lipid is present in the lipid solution at a concentration of about 30 mol % to about 50 mol %.

[0095] In some embodiments, the phospholipid lipid is present in the lipid solution at a concentration of about 5 mol % to about 15 mol %.

[0096] In some embodiments, the PEG lipid is present in the lipid solution at a concentration of about 0.1 mol % to about 1.0 mol %.

[0097] In some embodiments, the lipid solution comprises IL-1 at a concentration of about 30 mol % to about 70 mol %.

[0098] In some embodiments, the lipid solution comprises IL-2 at a concentration of about 30 mol % to about 70 mol %.

[0099] In some embodiments, the lipid solution comprises SL-2 at a concentration of 30 mol % to about 50 mol %.

[0100] In some embodiments, the lipid solution comprises DSPC at a concentration of about 5 mol % to about 15 mol %.

[0101] In some embodiments, the lipid solution comprises PEG2k-DMG at a concentration of about 0.1 mol % to about 1.0 mol %.

[0102] In some embodiments, the lipid solution comprises:(a) from about 30 mol % to about 70 mol % of ionizable lipid;(b) from 30 mol % to about 50 mol % of structural lipid;(c) from about 5 mol % to about 15 mol % of phospholipid; and(d) from about 0.1 mol % to about 1.0 mol % of PEG lipid.

[0103] In some embodiments, the lipid solution comprises:(a) from about 30 mol % to about 70 mol % of IL-1;(b) from 30 mol % to about 50 mol % of SL-2;(c) from about 5 mol % to about 15 mol % of DSPC; and(d) from about 0.1 mol % to about 1.0 mol % of PEG2k-DMG.

[0104] In some embodiments, the lipid solution comprises:(a) from about 30 mol % to about 70 mol % of IL-2;(b) from 30 mol % to about 50 mol % of SL-2;(c) from about 5 mol % to about 15 mol % of DSPC; and(d) from about 0.1 mol % to about 1.0 mol % of PEG2k-DMG.

[0105] In some embodiments, the lipid solution comprises ionizable lipid at a concentration of about 10 mg / mL to about 20 mg / mL.

[0106] In some embodiments, the lipid solution comprises structural lipid at a concentration of about 4 mg / mL to about 8 mg / mL.

[0107] In some embodiments, the lipid solution comprises phospholipid at a concentration of about 2 mg / mL to about 5 mg / mL.

[0108] In some embodiments, the lipid solution comprises PEG lipid at a concentration of about 0.1 mg / mL to about 1.0 mg / mL.

[0109] In some embodiments, the lipid solution comprises:(a) about 10 mg / mL to about 20 mg / mL of ionizable lipid;(b) about 4 mg / mL to about 8 mg / mL of structural lipid;(c) about 2 mg / mL to about 5 mg / mL of phospholipid; and(d) about 0.1 mg / mL to about 1.0 mg / mL of PEG lipid.

[0110] In some embodiments, the lipid solution comprises:(a) about 15±10 mg / mL, about 15±9 mg / mL, about 15±8 mg / mL, about 15±7 mg / mL, about 15±6 mg / mL, about 15±5 mg / mL, about 15±4 mg / mL, about 15±3 mg / mL, or about 15±2 mg / mL of ionizable lipid;(b) about 6±4 mg / mL, about 6±3 mg / mL, about 6±2 mg / mL, or about 6±1 mg / mL of structural lipid;(c) about 3.0±1.0 mg / mL, about 3.0±0.9 mg / mL, about 3.0±0.8 mg / mL, about 3.0±0.7 mg / mL, about 3.0±0.6 mg / mL, about 3.0±0.5 mg / mL, about 3.0±0.4 mg / mL, about 3.0±0.3 mg / mL, about 3.0±0.2 mg / mL, or about 3.0±0.1 mg / mL of phospholipid; and(d) about 0.5±0.4 mg / mL, about 0.5±0.3 mg / mL, about 0.5±0.2 mg / mL, or about 0.5±0.1 mg / mL of PEG lipid.[OHl] In some embodiments, the lipid solution comprises from about 10 mg / mL to about 20 mg / mL of IL-1.

[0112] In some embodiments, the lipid solution comprises from about 10 mg / mL to about 20 mg / mL of IL-2.

[0113] In some embodiments, the lipid solution comprises from about 4 mg / mL to about 8 mg / mL of SL-2.

[0114] In some embodiments, the lipid solution comprises from about 2 mg / mL to about 5 mg / mL of DSPC.

[0115] In some embodiments, the lipid solution comprises from about 0.1 mg / mL to about 1.0 mg / mL of PEG2k-DMG.

[0116] In some embodiments, the lipid solution comprises:(a) from about 10 mg / mL to about 20 mg / mL of IL-1;(b) from about 4 mg / mL to about 8 mg / mL of SL-2;(c) from about 2 mg / mL to about 5 mg / mL of DSPC; and(d) from about 0.1 mg / mL to about 1.0 mg / mL of PEG2k-DMG.

[0117] In some embodiments, the lipid solution comprises:(a) from about 10 mg / mL to about 20 mg / mL of IL-2;(b) from about 4 mg / mL to about 8 mg / mL of SL-2;(c) from about 2 mg / mL to about 5 mg / mL of DSPC; and(d) from about 0.1 mg / mL to about 1.0 mg / mL of PEG2k-DMG.

[0118] In some embodiments, the lipid solution comprises:(a) about 15±10 mg / mL, about 15±9 mg / mL, about 15±8 mg / mL, about 15±7 mg / mL, about 15±6 mg / mL, about 15±5 mg / mL, about 15±4 mg / mL, about 15±3 mg / mL, or about 15±2 mg / mL of IL-1;(b) about 6±4 mg / mL, about 6±3 mg / mL, about 6±2 mg / mL, or about 6±1 mg / mL of SL-2;(c) about 3.0±1.0 mg / mL, about 3.0±0.9 mg / mL, about 3.0±0.8 mg / mL, about 3.0±0.7 mg / mL, about 3.0±0.6 mg / mL, about 3.0±0.5 mg / mL, about 3.0±0.4 mg / mL, about 3.0±0.3 mg / mL, about 3.0±0.2 mg / mL, or about 3.0±0.1 mg / mL of DSPC; and(d) about 0.5±0.4 mg / mL, about 0.5±0.3 mg / mL, about 0.5±0.2 mg / mL, or about 0.5±0.1 mg / mL of PEG2k-DMG.

[0119] In some embodiments, the lipid solution comprises:(a) about 15±10 mg / mL, about 15±9 mg / mL, about 15±8 mg / mL, about 15±7 mg / mL, about 15±6 mg / mL, about 15±5 mg / mL, about 15±4 mg / mL, about 15±3 mg / mL, or about 15±2 mg / mL of IL-2;(b) about 6±4 mg / mL, about 6±3 mg / mL, about 6±2 mg / mL, or about 6±1 mg / mL of SL-2;(c) about 3.0±1.0 mg / mL, about 3.0±0.9 mg / mL, about 3.0±0.8 mg / mL, about 3.0±0.7 mg / mL, about 3.0±0.6 mg / mL, about 3.0±0.5 mg / mL, about 3.0±0.4 mg / mL, about 3.0±0.3 mg / mL, about 3.0±0.2 mg / mL, or about 3.0±0.1 mg / mL of DSPC; and(d) about 0.5±0.4 mg / mL, about 0.5±0.3 mg / mL, about 0.5±0.2 mg / mL, or about 0.5±0.1 mg / mL of PEG2k-DMG.First Aqueous Buffer Solution and First Buffering Agent

[0120] In some embodiments, the methods of the present disclosure provide first aqueous buffer solution comprising a first buffering agent.

[0121] In some embodiments, the first buffering agent is selected from ammonium sulfate, sodium bicarbonate, sodium citrate, sodium acetate, potassium phosphate, tri s(hydroxymethyl)aminom ethane (tris), sodium phosphate, and HEPES.

[0122] In some embodiments, the first buffering agent is phosphate.

[0123] In some embodiments, the first buffering agent is sodium phosphate.

[0124] In some embodiments, the first buffering agent is present in the first aqueous buffer solution at a concentration of from about 0.1 to about 100 mM, from about 0.5 to about 90 mM, from about 1.0 to about 80 mM, from about 2 to about 70 mM, from about 3 to about 60 mM, from about 4 to about 50 mM, from about 5 to about 40 mM, from about 6 to about 30 mM, from about 7 to about 20 mM, from about 8 to about 15 mM, or from about 9 to about 12 mM.

[0125] In some embodiments, the first buffering agent is present in the first aqueous buffer solution at a concentration of or greater than about 0.1 mM, 0.5 mM, 1 mM, 2 mM, 4 mM, 6 mM, 8 mM, 10 mM, 15 mM, 20 mM, 25 mM, 30 mM, 35 mM, 40 mM, 45 mM, or 50 mM.

[0126] In some embodiments, the first buffering agent is present in the first aqueous buffer solution at a concentration of 5.0±2.0 mM, 5.0±1.5 mM, 5.0±1.0 mM, 5.0±0.9 mM, 5.0±0.8 mM, 5.0±0.7 mM, 5.0±0.6 mM, 5.0±0.5 mM, 5.0±0.4 mM, 5.0±0.3 mM, 5.0±0.2 mM, or 5.0±0.1 mM.

[0127] In some embodiments, the first aqueous buffer solution has a pH of 11.0±3.0, about 11.0±2.0, about 11.0±1.5, about 11.0±1.0, about 11.0±0.9, about 11.0±0.8, about 11.0±0.7,about 11.0±0.6, about 11.0±0.5, about 11.0±0.4, about 11.0±0.3, about 11.0±0.2, or about 11.0±0.1 (e.g., about 11.6).

[0128] In some embodiments, the first aqueous buffer solution is selected from an acetate buffer, a citrate buffer, a phosphate buffer, and a tris buffer.

[0129] In some embodiments, the aqueous buffer solution comprises a phosphate buffer.Holding Step

[0130] In some embodiments, the methods of the present disclosure provide a holding step, comprising holding the intermediate empty -LNP solution for a residence time.

[0131] In some embodiments, the residence time is less than about 1 second.

[0132] In some embodiments, the residence time is about 1 second, about 2 seconds, about 3 seconds, about 4 seconds, about 5 seconds, about 6 seconds, about 7 seconds, about 8 seconds, about 9 seconds, about 10 seconds, about 11 seconds, about 12 seconds, about 13 seconds, about 14 seconds, about 15 seconds, about 16 seconds, about 17 seconds, about 18 seconds, about 19 seconds, about 20 seconds, about 30 seconds, about 40 seconds, about 50 seconds, or about 1 minute.

[0133] In some embodiments, the residence time is about 30±20 seconds, about 30±15 seconds, about 30±10 seconds, about 30±9 seconds, about 30±8 seconds, about 30±7 seconds, about 30±6 seconds, about 30±5 seconds, about 30±4 seconds, about 30±3 seconds, about 30±2 seconds, about 30±l seconds (e.g., about 30 seconds).

[0134] In some embodiments, the residence time is about 15±10 seconds, about 15±9 seconds, about 15±8 seconds, about 15±7 seconds, about 15±6 seconds, about 15±5 seconds, about 15±4 seconds, about 15±3 seconds, about 15±2 seconds, about 15±1 seconds (e.g., about 15 seconds).

[0135] In some embodiments, the residence time is about 10±5 seconds, about 10±4 seconds, about 10±3 seconds, about 10±2 seconds, about 10±l seconds (e.g., about 10 seconds).

[0136] In some embodiments, the residence time is about 5±3 seconds, about 5±2 seconds, about 5±1 seconds (e.g., about 5 seconds).

[0137] In some embodiments, the residence time is about 1 minute, about 2 minutes, about 3 minutes, about 4 minutes, about 5 minutes, about 6 minutes, about 7 minutes, about 8 minutes, about 9 minutes, about 10 minutes, about 11 minutes, about 12 minutes, about 13 minutes, about 14 minutes, about 15 minutes, about 16 minutes, about 17 minutes, about 18 minutes, about 19 minutes, about 20 minutes, about 30 minutes, about 40 minutes, about 50 minutes, or about 1 hour.

[0138] In some embodiments, the residence time is configured such that the average diameter of the empty LNP is about 1%, about 2%, about 3%, about 4%, about 5%, about 10%, about 20%, about 30%, about 40%, about 50%, about 60%, about 70%, about 80%, about 90%, about 100%, about 150%, about 200%, about 250%, about 300%, about 350%, about 400%, about 450%, about 500%, about 600%, about 700%, about 800%, about 900%, or about 1000% greater than the average diameter of the intermediate empty LNP.

[0139] In some embodiments, the residence time is configured such that the average diameter of the empty LNP is greater than the average diameter of the intermediate empty LNP by about 1 nm, about 2 nm, about 3 nm, about 4 nm, about 5 nm, about 10 nm, about 20 nm, about 30 nm, about 40 nm, about 50 nm, about 60 nm, about 70 nm, about 80 nm, about 90 nm, or about 100 nm.

[0140] In some embodiments, the residence time is configured such that the average diameter of the empty LNP is from about 50 nm to about 70 nm.

[0141] In some embodiments, the residence time is configured such that the average diameter of the empty LNP is about 60±30 nm, about 60±20 nm, about 60±15 nm, about 60±10 nm, about 60±9 nm, about 60±8 nm, about 60±7 nm, about 60±6 nm, about 60±5 nm, about 60±4 nm, about 60±3 nm, about 60±2 nm, or about 60±l nm.

[0142] In some embodiments, the residence time is configured such that the average diameter of the empty LNP is about 50±30 nm, about 50±20 nm, about 50±15 nm, about 50±10 nm, about 50±9 nm, about 50±8 nm, about 50±7 nm, about 50±6 nm, about 50±5 nm, about 50±4 nm, about 50±3 nm, about 50±2 nm, or about 50±l nm.Diluting Step

[0143] In some embodiments, the methods of the present disclosure provides a diluting step, comprising adding a diluting solution to the intermediate empty -LNP solution, thereby forming the empty -LNP solution comprising an empty LNP.

[0144] In some embodiments, the diluting solution is an aqueous solution.

[0145] In some embodiments, the diluting solution is a second aqueous buffer solution comprising a second buffering agent.

[0146] In some embodiments, the second buffering agent is selected from ammonium sulfate, sodium bicarbonate, sodium citrate, sodium acetate, potassium phosphate, tri s(hydroxymethyl)aminom ethane (tris), sodium phosphate, and HEPES.

[0147] In some embodiments, the second buffering agent is phosphate.

[0148] In some embodiments, the second buffering agent is sodium phosphate.

[0149] In some embodiments, the second buffering agent is present in the second aqueous buffer solution at a concentration of from about 0.1 to about 100 mM, from about 0.5 to about 90 mM, from about 1.0 to about 80 mM, from about 2 to about 70 mM, from about 3 to about 60 mM, from about 4 to about 50 mM, from about 5 to about 40 mM, from about 6 to about 30 mM, from about 7 to about 20 mM, from about 8 to about 15 mM, or from about 9 to about 12 mM.

[0150] In some embodiments, the second buffering agent is present in the second aqueous buffer solution at a concentration of or greater than about 0.1 mM, 0.5 mM, 1 mM, 2 mM, 4 mM, 6 mM, 8 mM, 10 mM, 15 mM, 20 mM, 25 mM, 30 mM, 35 mM, 40 mM, 45 mM, or 50 mM.

[0151] In some embodiments, the second buffering agent is present in the second aqueous buffer solution at a concentration of 5.0±2.0 mM, 5.0±1.5 mM, 5.0±1.0 mM, 5.0±0.9 mM, 5.0±0.8 mM, 5.0±0.7 mM, 5.0±0.6 mM, 5.0±0.5 mM, 5.0±0.4 mM, 5.0±0.3 mM, 5.0±0.2 mM, or 5.0±0.1 mM.

[0152] In some embodiments, the second buffering agent is the same as the first buffering agent (e.g., the first and second buffering agents are phosphate (e.g., sodium phosphate)).

[0153] In some embodiments, the second buffering agent is different from the first buffering agent (e.g., the first buffering agent is phosphate (e.g., sodium phosphate), and the second buffering agent is acetate (e.g., sodium acetate)).

[0154] In some embodiments, the pH value of diluting solution is substantially same as the pH value of the first aqueous solution comprising the first buffering agent.

[0155] In some embodiments, the diluting solution has a pH value being higher than the pKa value of the ionizable lipid.

[0156] In some embodiments, the pH value of diluting solution has a pH of 11 ,0±3.0, 11 ,0±2.0, 11.0±1.5, 11.0±1.0, 11.0±0.9, 11.0±0.8, 11.0±0.7, 11.0±0.6, 11.0±0.5, 11.0±0.4, 11.0±0.3, 11.0±0.2, or 11.0±0.1 (e.g., about 11.6).

[0157] In some embodiments, the second buffering agent is acetate.

[0158] In some embodiments, the second buffering agent is sodium acetate.

[0159] In some embodiments, the second buffering agent is present in the second aqueous buffer solution at a concentration of from about 0.1 to about 100 mM, from about 0.5 to about 90 mM, from about 1.0 to about 80 mM, from about 2 to about 70 mM, from about 3 to about 60 mM, from about 4 to about 50 mM, from about 5 to about 40 mM, from about 6 to about 30 mM, from about 7 to about 20 mM, from about 8 to about 15 mM, or from about 9 to about 12 mM.

[0160] In some embodiments, the second buffering agent is present in the second aqueous buffer solution at a concentration of or greater than about 0.1 mM, 0.5 mM, 1 mM, 2 mM, 4 mM, 6 mM, 8 mM, 10 mM, 15 mM, 20 mM, 25 mM, 30 mM, 35 mM, 40 mM, 45 mM, or 50 mM.

[0161] In some embodiments, the second buffering agent is present in the second aqueous buffer solution at a concentration of 5.0±2.0 mM, 5.0±1.5 mM, 5.0±1.0 mM, 5.0±0.9 mM, 5.0±0.8 mM, 5.0±0.7 mM, 5.0±0.6 mM, 5.0±0.5 mM, 5.0±0.4 mM, 5.0±0.3 mM, 5.0±0.2 mM, or 5.0±0.1 mM.

[0162] In some embodiments, the pH value of diluting solution is lower than the pH value of the aqueous solution comprising the first buffering agent.

[0163] In some embodiments, the pH value of diluting solution is lower than the pKa of the ionizable lipid in the empty LNP.

[0164] In some embodiments, the pH value of diluting solution is lower than the pH value of the aqueous solution comprising the first buffering agent by about 7.0±2.0, 7.0±1.5, 7.0±1.0, 7.0±0.9, 7.0±0.8, 7.0±0.7, 7.0±0.6, 7.0±0.5, 7.0±0.4, 7.0±0.3, 7.0±0.2, or 7.0±0.1.

[0165] In some embodiments, the pH value of diluting solution is about 5.0±2.0, 5.0±1.5, 5.0±1.0, 5.0±0.9, 5.0±0.8, 5.0±0.7, 5.0±0.6, 5.0±0.5, 5.0±0.4, 5.0±0.3, 5.0±0.2, or 5.0±0.1 (e.g., about 4.4).

[0166] In some embodiments, the diluting solution is selected from an acetate buffer, a citrate buffer, a phosphate buffer, and a tris buffer.

[0167] In some embodiments, the diluting solution comprises acetate buffer.

[0168] In some embodiments, the diluting solution comprises acetate buffer having a pH lower than the pKa of the ionizable lipid in the empty LNP.

[0169] In some embodiments, the diluting solution comprises acetate buffer having a pH at about 5.0.

[0170] In some embodiments, the diluting solution comprises about 5 mM acetate buffer at about pH 5.0.

[0171] In some embodiments, the diluting solution further comprises a PEG lipid.

[0172] In some embodiments, the diluting solution is free of PEG lipid.

[0173] In some embodiments, the diluting solution has a pH value being higher than the pKa value of the ionizable lipid, and diluting solution further comprises a PEG lipid.

[0174] In some embodiments, the diluting solution has a pH value being higher than the pKa value of the ionizable lipid, and diluting solution is free of PEG lipid.

[0175] In some embodiments, the diluting solution has a pH value being lower than the pKa value of the ionizable lipid, and the diluting solution further comprises a PEG lipid.

[0176] In some embodiments, the diluting solution has a pH value being lower than the pKa value of the ionizable lipid, and the diluting solution is free of PEG lipid.Empty Lipid Nanoparticle Solution and Formulation (Empty-LNP Solutions and Empty-LNP Formulation)

[0177] In some embodiments, the methods of the present disclosure provide an empty lipid nanoparticle solution (empty-LNP solution) being prepared by a method disclosed herein.

[0178] In some embodiments, the methods of the present disclosure provide an empty lipid nanoparticle formulation (empty-LNP formulation) being prepared by a method disclosed herein.

[0179] In some embodiments, the empty-LNP solution has a pH being lower than the pKa of the ionizable lipid.

[0180] In some embodiments, the empty-LNP solution has a pH being lower than the pKa of the ionizable lipid, and the empty-LNP solution is free of PEG lipid.

[0181] In some embodiments, the empty-LNP solution comprise the empty LNP. In some embodiments, the empty-LNP solution comprises the empty LNP at a concentration of greater than about 0.01 mg / mL, 0.05 mg / mL, 0.06 mg / mL, 0.07 mg / mL, 0.08 mg / mL, 0.09 mg / mL, 0.1 mg / mL, 0.15 mg / mL, 0.2 mg / mL, 0.3 mg / mL, 0.4 mg / mL, 0.5 mg / mL, 0.6 mg / mL, 0.7 mg / mL, 0.8 mg / mL, 0.9 mg / mL, or 1.0 mg / mL. In some embodiments, the empty-LNP solution comprises the empty LNP at a concentration ranging from about 0.01-1.0 mg / mL, 0.01-0.9 mg / mL, 0.01-0.8 mg / mL, 0.01-0.7 mg / mL, 0.01-0.6 mg / mL, 0.01-0.5 mg / mL, 0.01- 0.4 mg / mL, 0.01-0.3 mg / mL, 0.01-0.2 mg / mL, 0.01-0.1 mg / mL, 0.05-1.0 mg / mL, 0.05-0.9 mg / mL, 0.05-0.8 mg / mL, 0.05-0.7 mg / mL, 0.05-0.6 mg / mL, 0.05-0.5 mg / mL, 0.05-0.4 mg / mL, 0.05-0.3 mg / mL, 0.05-0.2 mg / mL, 0.05-0.1 mg / mL, 0.1-1.0 mg / mL, 0.2-0.9 mg / mL, 0.3-0.8 mg / mL, 0.4-0.7 mg / mL, or 0.5-0.6 mg / mL. In some embodiments, the empty-LNP solution comprises an empty LNP at a concentration up to about 5.0 mg / mL, 4.0 mg / mL, 3.0 mg / mL, 2.0 mg / mL, 1.0 mg / mL, 0.09 mg / mL, 0.08 mg / mL, 0.07 mg / mL, 0.06 mg / mL, or 0.05 mg / mL.

[0182] In some embodiments, the empty-LNP solution comprises about 5.0±2.0 mM, 5.0±1.5 mM, 5.0±1.0 mM, 5.0±0.9 mM, 5.0±0.8 mM, 5.0±0.7 mM, 5.0±0.6 mM, 5.0±0.5 mM, 5.0±0.4 mM, 5.0±0.3 mM, 5.0±0.2 mM, or 5.0±0.1 mM citrate, acetate, phosphate or tris.

[0183] In some embodiments, the empty-LNP solution about 5.2±2.0 mM, 5.2±1.5 mM, 5.2±1.0 mM, 5.2±0.9 mM, 5.2±0.8 mM, 5.2±0.7 mM, 5.2±0.6 mM, 5.2±0.5 mM, 5.2±0.4 mM, 5.2±0.3 mM, 5.2±0.2 mM, or 5.2±0.1 mM acetate.

[0184] In some embodiments, the empty-LNP solution may have a pH of 5.2±2.0, 5.2±1.5, 5.2±1.0, 5.2±0.9, 5.2±0.8, 5.2±0.7, 5.2±0.6, 5.2±0.5, 5.2±0.4, 5.2±0.3, 5.2±0.2, or 5.2±0.1.

[0185] In some embodiments, the empty-LNP solution comprises acetate buffer having a pH of 5.2±2.0, 5.2±L5, 5.2±1.0, 5.2±0.9, 5.2±0.8, 5.2±0.7, 5.2±0.6, 5.2±0.5, 5.2±0.4, 5.2±0.3, 5.2±0.2, or 5.2±0.1.

[0186] In some embodiments, the empty-LNP solution comprises about 5 mM citrate, acetate, phosphate, or tris.

[0187] In some embodiments, the empty-LNP solution comprises acetate.

[0188] In some embodiments, the empty-LNP solution comprises about 5 mM acetate.

[0189] In some embodiments, the empty-LNP solution comprises acetate having a pH of about 5.2.

[0190] In some embodiments, the empty-LNP solution comprises about 5 mM acetate, wherein the aqueous buffer solution has a pH of about 5.2.

[0191] In some embodiments, the empty-LNP formulation has a pH being higher than the pKa of the ionizable lipid.

[0192] In some embodiments, the empty-LNP formulation has a pH being higher than the pKa of the ionizable lipid, and the empty-LNP solution comprises PEG lipid.Empty Lipid Nanoparticles (Empty LNPs)

[0193] In some embodiments, the methods of the present disclosure provide an empty LNP comprising an ionizable lipid, a structural lipid, and a phospholipid.

[0194] In some embodiments, the methods of the present disclosure provide an empty LNP comprising an ionizable lipid, a structural lipid, a phospholipid, and a phosphatidylserine phospholipid.

[0195] In some embodiments, the empty LNPs comprises a PEG lipid.

[0196] In some embodiments, the empty LNPs is free of PEG lipid.

[0197] In some embodiments, the empty LNPs comprises from about 30 mol % to about 70 mol % of ionizable lipid.

[0198] In some embodiments, the empty LNPs comprises from about 30 mol % to about 50 mol % of structural lipid.

[0199] In some embodiments, the empty LNPs comprises from about 5 mol % to about 15 mol % of phospholipid lipid.

[0200] In some embodiments, the empty LNPs comprises from about 0.1 mol % to about 5.0 mol % of PEG lipid.

[0201] In some embodiments, the empty LNPs comprises from about 1.0 mol % to about 8.0 mol % of phosphatidylserine phospholipid.

[0202] In some embodiments, the empty LNPs comprises from about 30 mol % to about 70 mol % of IL-1.

[0203] In some embodiments, the empty LNPs comprises from about 30 mol % to about 70 mol % of IL-2.

[0204] In some embodiments, the empty LNPs comprises from about 30 mol % to about 50 mol % of SL-2.

[0205] In some embodiments, the empty LNPs comprises from about 5 mol % to about 15 mol % of DSPC.

[0206] In some embodiments, the empty LNPs comprises from about 0.1 mol % to about 5.0 mol % of PEG2k-DMG.

[0207] In some embodiments, the empty LNPs comprises from about 1.0 mol % to about 8.0 mol % of DMPS.

[0208] In some embodiments, the empty LNPs comprises:(a) from about 30 mol % to about 70 mol % of ionizable lipid;(b) from about 30 mol % to about 50 mol % of structural lipid;(c) from about 5 mol % to about 15 mol % of phospholipid; and(d) from about 0.1 mol % to about 5.0 mol % of PEG lipid.

[0209] In some embodiments, the empty LNPs comprises:(a) from about 30 mol % to about 70 mol % of ionizable lipid;(b) from about 30 mol % to about 50 mol % of structural lipid;(c) from about 5 mol % to about 15 mol % of phospholipid;(d) from about 0.1 mol % to about 5.0 mol % of PEG lipid; and(e) from about 1.0 mol % to about 8.0 mol % of phosphatidylserine phospholipid.

[0210] In some embodiments, the empty LNPs comprises:(a) IL-l;(b) SL-2;(c) DSPC; and(d) PEG2k-DMG.

[0211] In some embodiments, the empty LNPs comprises:(a) IL-l;(b) SL-2;(c) DSPC;(d) PEG2k-DMG; and(e) DMPS.

[0212] In some embodiments, the empty LNPs comprises:(a) IL-2;(b) SL-2;(c) DSPC; and(d) PEG2k-DMG.

[0213] In some embodiments, the empty LNPs comprises:(a) IL-2;(b) SL-2;(c) DSPC;(d) PEG2k-DMG; and(e) DMPS.

[0214] In some embodiments, the empty LNPs comprises:(a) from about 30 mol % to about 70 mol % of IL-1;(b) from about 30 mol % to about 50 mol % of SL-2;(c) from about 5 mol % to about 15 mol % of DSPC;(d) from about 0.1 mol % to about 5.0 mol % of PEG2k-DMG; and(e) from about 1.0 mol % to about 8.0 mol % of DMPS.

[0215] In some embodiments, the empty LNPs comprises:(a) from about 30 mol % to about 70 mol % of IL-2;(b) from about 30 mol % to about 50 mol % of SL-2;(c) from about 5 mol % to about 15 mol % of DSPC;(d) from about 0.1 mol % to about 5.0 mol % of PEG2k-DMG; and(e) from about 1.0 mol % to about 8.0 mol % of DMPS

[0216] In some embodiments, the empty LNP comprises about 30-60 mol% IL-1; about 0-30 mol% DSPC; about 15-50 mol% SL-2; and about 0.1-0.5 mol% PEG2k-DMG. In some embodiments, the empty LNP comprises about 0-30 mol% DSPC; about 15-50 mol% SL-2; and about 0.1 -0.5 mol% PEG2k-DMG. In some embodiments, the empty LNP comprises about 30-60 mol% IL-1; about 15-50 mol% SL-2; and about 0.1-0.5 mol% PEG2k-DMG. In someembodiments, the empty LNP comprises about 30-60 mol% IL-1; about 0-30 mol% DSPC; and about 0.1 -0.5 mol% PEG2k-DMG. In some embodiments, the empty LNP comprises about 30-60 mol% IL-1; about 0-30 mol% DSPC; and about 15-50 mol% SL-2. In some embodiments, the empty LNP comprises about 30-60 mol% IL-1 and about 0.1-0.5 mol% PEG2k-DMG. In some embodiments, the empty LNP comprises about 30-60 mol% IL-1 and about 0-30 mol% DSPC. In some embodiments, the empty LNP comprises about 30-60 mol% IL-1 and about 15-50 mol% SL-2. In some embodiments, the empty LNP comprises about 0- 30 mol% DSPC and about 15-50 mol% SL-2. In some embodiments, the empty LNP comprises about 0-30 mol% DSPC and about 0.1-0.5 mol% PEG2k-DMG. In some embodiments, the empty LNP comprises about about 15-50 mol% SL-2 and about 0.1-0.5 mol% PEG2k-DMG. In some embodiments, the empty LNP comprises about 30-60 mol% IL-1. In some embodiments, the empty LNP comprises about 0-30 mol% DSPC. In some embodiments, the empty LNP comprises about 15-50 mol% SL-2. In some embodiments, the empty LNP comprises about 0.1-0.5 mol% PEG2k-DMG.

[0217] In some embodiments, the empty LNP comprises about 30-60 mol% IL-2; about 0-30 mol% DSPC; about 15-50 mol% SL-2; and about 0.1-0.5 mol% PEG2k-DMG. In some embodiments, the empty LNP comprises about 0-30 mol% DSPC; about 15-50 mol% SL-2; and about 0.1 -0.5 mol% PEG2k-DMG. In some embodiments, the empty LNP comprises about 30-60 mol% IL-2; about 15-50 mol% SL-2; and about 0.1-0.5 mol% PEG2k-DMG. In some embodiments, the empty LNP comprises about 30-60 mol% IL-2; about 0-30 mol% DSPC; and about 0.1 -0.5 mol% PEG2k-DMG. In some embodiments, the empty LNP comprises about 30-60 mol% IL-2; about 0-30 mol% DSPC; and about 15-50 mol% SL-2. In some embodiments, the empty LNP comprises about 30-60 mol% IL-2 and about 0.1-0.5 mol% PEG2k-DMG. In some embodiments, the empty LNP comprises about 30-60 mol% IL-2 and about 0-30 mol% DSPC. In some embodiments, the empty LNP comprises about 30-60 mol% IL-2 and about 15-50 mol% SL-2. In some embodiments, the empty LNP comprises about 0- 30 mol% DSPC and about 15-50 mol% SL-2. In some embodiments, the empty LNP comprises about 0-30 mol% DSPC and about 0.1-0.5 mol% PEG2k-DMG. In some embodiments, the empty LNP comprises about about 15-50 mol% SL-2 and about 0.1-0.5 mol% PEG2k-DMG. In some embodiments, the empty LNP comprises about 30-60 mol% IL-2. In some embodiments, the empty LNP comprises about 0-30 mol% DSPC. In some embodiments, the empty LNP comprises about 15-50 mol% SL-2. In some embodiments, the empty LNP comprises about 0.1-0.5 mol% PEG2k-DMG.

[0218] In some embodiments, the empty LNP comprises about 30-60 mol% IL-1; about 0-30 mol% DSPC; about 15-50 mol% SL-2; and about 0.1-10 mol% PEG2k-DMG. In some embodiments, the empty LNP comprises about 0-30 mol% DSPC; about 15-50 mol% SL-2; and about 0.1-10 mol% PEG2k-DMG. In some embodiments, the empty LNP comprises about 0-30 mol% DSPC; about 15-50 mol% SL-2; and about 0.1-10 mol% PEG2k-DMG. In some embodiments, the empty LNP comprises about 30-60 mol% IL-1; about 15-50 mol% SL-2; and about 0.1-10 mol% PEG2k-DMG. In some embodiments, the empty LNP comprises about 30-60 mol% IL-1; about 0-30 mol% DSPC; and about 0.1-10 mol% PEG2k-DMG. In some embodiments, the empty LNP comprises about 30-60 mol% IL-1; about 0-30 mol% DSPC; and about 15-50 mol% SL-2. In some embodiments, the empty LNP comprises about 30-60 mol% IL-1 and about 0-30 mol% DSPC. In some embodiments, the empty LNP comprises about 30-60 mol% IL-1 and about 15-50 mol% SL-2. In some embodiments, the empty LNP comprises about 30-60 mol% IL-1 and about 0.1-10 mol% PEG2k-DMG. In some embodiments, the empty LNP comprises about 0-30 mol% DSPC and about 15-50 mol% SL- 2. In some embodiments, the empty LNP comprises about 0-30 mol% DSPC about 0.1-10 mol% PEG2k-DMG. In some embodiments, the empty LNP comprises about 15-50 mol% SL- 2 and about 0.1-10 mol% PEG2k-DMG. In some embodiments, the empty LNP comprises about 30-60 mol% IL-1. In some embodiments, the empty LNP comprises about 0-30 mol% DSPC. In some embodiments, the empty LNP comprises about 15-50 mol% SL-2. In some embodiments, the empty LNP comprises about 0.1-10 mol% PEG2k-DMG.

[0219] In some embodiments, the empty LNP comprises about 30-60 mol% IL-2; about 0-30 mol% DSPC; about 15-50 mol% SL-2; and about 0.1-10 mol% PEG2k-DMG. In some embodiments, the empty LNP comprises about 0-30 mol% DSPC; about 15-50 mol% SL-2; and about 0.1-10 mol% PEG2k-DMG. In some embodiments, the empty LNP comprises about 0-30 mol% DSPC; about 15-50 mol% SL-2; and about 0.1-10 mol% PEG2k-DMG. In some embodiments, the empty LNP comprises about 30-60 mol% IL-2; about 15-50 mol% SL-2; and about 0.1-10 mol% PEG2k-DMG. In some embodiments, the empty LNP comprises about 30-60 mol% IL-2; about 0-30 mol% DSPC; and about 0.1-10 mol% PEG2k-DMG. In some embodiments, the empty LNP comprises about 30-60 mol% IL-2; about 0-30 mol% DSPC; and about 15-50 mol% SL-2. In some embodiments, the empty LNP comprises about 30-60 mol% IL-2 and about 0-30 mol% DSPC. In some embodiments, the empty LNP comprises about 30-60 mol% IL-2 and about 15-50 mol% SL-2. In some embodiments, the empty LNP comprises about 30-60 mol% IL-2 and about 0.1-10 mol% PEG2k-DMG. In some embodiments, the empty LNP comprises about 0-30 mol% DSPC and about 15-50 mol% SL-2. In some embodiments, the empty LNP comprises about 0-30 mol% DSPC about 0.1-10 mol% PEG2k-DMG. In some embodiments, the empty LNP comprises about 15-50 mol% SL- 2 and about 0.1-10 mol% PEG2k-DMG. In some embodiments, the empty LNP comprises about 30-60 mol% IL-2. In some embodiments, the empty LNP comprises about 0-30 mol% DSPC. In some embodiments, the empty LNP comprises about 15-50 mol% SL-2. In some embodiments, the empty LNP comprises about 0.1-10 mol% PEG2k-DMG.

[0220] In some embodiments, the empty LNP has an average lipid nanoparticle diameter of about 200 nm, about 175 nm, about 150 nm, about 125 nm, about 100 nm, about 90 nm, about 80 nm, about 75 nm, about 70 nm, about 65 nm, about 60 nm, about 55 nm, about 50 nm, about 45 nm, about 40 nm, about 35 nm, about 30 nm, about 25 nm, or about 20 nm (for example, as measured by dynamic light scattering).

[0221] In some embodiments, the empty LNP has an average lipid nanoparticle diameter of about 200 nm or less, about 175 nm or less, about 150 nm or less, about 125 nm or less, about 100 nm or less, about 90 nm or less, about 80 nm or less, about 75 nm or less, about 70 nm or less, about 65 nm or less, about 60 nm or less, about 55 nm or less, about 50 nm or less, about 45 nm or less, about 40 nm or less, about 35 nm or less, about 30 nm or less, about 25 nm or less, or about 20 nm or less (for example, as measured by dynamic light scattering).

[0222] In some embodiments, the empty LNP has an average lipid nanoparticle diameter of about 20 nm to about 150 nm, about 25 nm to about 125 nm, about 30 nm to about 110 nm, about 35 nm to about 100 nm, about 40 nm to about 90 nm, about 45 nm to about 80 nm, or about 50 nm to about 70 nm (for example, as measured by dynamic light scattering).

[0223] In some embodiments, empty LNP has an average lipid nanoparticle diameter of about 25 to about 45 nm (for example, as measured by dynamic light scattering).Loading Step

[0224] In some embodiments, the methods of the present disclosure provide a loading step, comprising mixing a nucleic acid solution comprising a nucleic acid with the empty-LNP solution or empty-LNP formulation, thereby forming a loaded lipid nanoparticle solution (loaded-LNP solution) comprising a loaded LNP.

[0225] In some embodiments, the empty-LNP solution or empty-LNP formulation is subjected to the loading step without holding or storage.

[0226] In some embodiments, the empty-LNP solution or empty-LNP formulation is subjected to the loading step after holding for a period of time.

[0227] In some embodiments, the empty -LNP solution or empty -LNP formulation is subjected to the loading step after holding for about 1 minute, about 2 minutes, about 3 minutes, about 4 minutes, about 5 minutes, about 10 minutes, about 20 minutes, about 30 minutes, about 40 minutes, about 50 minutes, about 1 hour, about 2 hours, about 3 hours, about 4 hours, about 5 hours, about 6 hours, about 7 hours, about 8 hours, about 9 hours, about 10 hours, about 11 hours, about 12 hours, about 18 hours, or about 24 hours.

[0228] In some embodiments, the empty -LNP solution or empty -LNP formulation is subjected to the loading step after storage for about 1 hour, about 2 hours, about 3 hours, about 4 hours, about 5 hours, about 6 hours, about 7 hours, about 8 hours, about 9 hours, about 10 hours, about 11 hours, about 12 hours, about 18 hours, about 1 day, about 2 days, about 3 days, about 4 days, about 5 days, about 6 days, about 1 week, about 2 weeks, about 3 weeks, about 1 month, about 2 months, about 3 months, about 4 months, about 5 months, about 6 months, about 7 months, about 8 months, about 9 months, about 10 months, about 11 months, about 1 year, about 2 years, about 3 years, about 4 years, or about 5 years.

[0229] In some embodiments, upon formation, the empty-LNP solution or empty-LNP formulation is subjected to the loading step without storage or holding for a period of time.

[0230] In some embodiments, the loading step is performed with a T-junction, confined impinging jets, microfluidic mixer, or vortex mixer.

[0231] In some embodiments, the loading step is performed under a pH of about 4.5±1.5, 4.5±1.4, 4.5±1.3, 4.5±1.2, 4.5±1.1, 4.5±1.0, 4.5±0.9, 4.5±0.8, 4.5±0.7, 4.5±0.6, 4.5±0.5, 4.5±0.4, 4.5±0.3, 4.5±0.2, or 4.5±0.1.

[0232] In some embodiments, the methods of the present disclosure further comprise: iv) processing the loaded-LNP solution, thereby forming a loaded lipid nanoparticle formulation (loaded-LNP formulation) comprising a loaded lipid nanoparticle (loaded LNP).

[0233] In some embodiments, the step of processing the loaded-LNP solution comprises a first adding step, comprising adding a polyethylene glycol lipid (PEG lipid) to the loaded LNP solution.

[0234] In some embodiments, the step of processing the loaded-LNP solution further comprises a second adding step, comprising adding a polyethylene glycol lipid (PEG lipid) to the loaded LNP solution.

[0235] In some embodiments, first adding step comprises adding about 0.1 mol% to about 3.0 mol%, about 0.2 mol% to about 2.5 mol%, about 0.5 mol% to about 2.0 mol%, about 0.75 mol% to about 1.5 mol%, about 1.0 mol% to about 1.25 mol% PEG lipid to the loaded-LNP solution.

[0236] In some embodiments, the first adding step comprises adding about 0.1 mol% to about 3.0 mol%, about 0.2 mol% to about 2.5 mol%, about 0.5 mol% to about 2.0 mol%, about 0.75 mol% to about 1.5 mol%, about 1.0 mol% to about 1.25 mol% PEG lipid to the loaded-LNP solution.

[0237] In some embodiments, the first adding step comprises adding about 0.1 mol%, about 0.2 mol%, about 0.3 mol%, about 0.4 mol%, about 0.5 mol%, about 0.6 mol%, about 0.7 mol%, about 0.8 mol%, about 0.9 mol%, about 1.0 mol%, about 1.1 mol%, about 1.2 mol%, about 1.3 mol%, about 1.4 mol%, about 1.5 mol%, about 1.6 mol%, about 1.7 mol%, about 1.8 mol%, about 1.9 mol%, about 2.0 mol%, about 2.1 mol%, about 2.2 mol%, about 2.3 mol%, about 2.4 mol%, about 2.5 mol%, about 2.6 mol%, about 2.7 mol%, about 2.8 mol%, about 2.9 mol%, or about 3.0 mol% of PEG lipid (e.g., PEG2k-DMG) to the loaded-LNP solution.

[0238] In some embodiments, the first adding step comprises adding about 1.75±0.5 mol%, about 1.75±0.4 mol%, about 1.75±0.3 mol%, about 1.75±0.2 mol%, or about 1.75±0.1 mol% (e.g., about 1.75 mol%) of PEG lipid (e.g., PEG2k-DMG) to the loaded-LNP solution.

[0239] In some embodiments, after the first adding step, the loaded LNP solution comprises about 1.0 mol%, about 1.1 mol%, about 1.2 mol%, about 1.3 mol%, about 1.4 mol%, about 1.5 mol%, about 1.6 mol%, about 1.7 mol%, about 1.8 mol%, about 1.9 mol%, about 2.0 mol%, about 2.1 mol%, about 2.2 mol%, about 2.3 mol%, about 2.4 mol%, about 2.5 mol%, about 2.6 mol%, about 2.7 mol%, about 2.8 mol%, about 2.9 mol%, about 3.0 mol%, about 3.1 mol%, about 3.2 mol%, about 3.3 mol%, about 3.4 mol%, about 3.5 mol%, about 3.6 mol%, about 3.7 mol%, about 3.8 mol%, about 3.9 mol%, about 4.0 mol%, about 4.1 mol%, about 4.2 mol%, about 4.3 mol%, about 4.4 mol%, about 4.5 mol%, about 4.6 mol%, about 4.7 mol%, about 4.8 mol%, about 4.9 mol%, or about 5.0 mol% of PEG lipid (e.g., PEG2k-DMG).

[0240] In some embodiments, the second adding step comprises adding a PEG.

[0241] In some embodiments, the second adding step comprises adding about 0.1 mol% to about 3.0 mol% PEG, about 0.2 mol% to about 2.5 mol% PEG, about 0.5 mol% to about 2.0 mol% PEG, about 0.75 mol% to about 1.5 mol% PEG, about 1.0 mol% to about 1.25 mol% PEG to the loaded LNP solution.

[0242] In some embodiments, the second adding step comprises adding about 0.1 mol%, about 0.2 mol%, about 0.3 mol%, about 0.4 mol%, about 0.5 mol%, about 0.6 mol%, about 0.7 mol%, about 0.8 mol%, about 0.9 mol%, about 1.0 mol%, about 1.1 mol%, about 1.2 mol%, about 1.3 mol%, about 1.4 mol%, about 1.5 mol%, about 1.6 mol%, about 1.7 mol%, about 1.8 mol%, about 1.9 mol%, about 2.0 mol%, about 2.1 mol%, about 2.2 mol%, about 2.3 mol%, about 2.4mol%, about 2.5 mol%, about 2.6 mol%, about 2.7 mol%, about 2.8 mol%, about 2.9 mol%, or about 3.0 mol% of PEG lipid (e.g., PEG2k-DMG).

[0243] In some embodiments, the second adding step comprises adding about 1.0±0.5 mol%, about 1.0±0.4 mol%, about 1.0±0.3 mol%, about 1.0±0.2 mol%, or about 1.0±0.1 mol% (e.g., about 1.0 mol%) of PEG lipid (e.g., PEG2k-DMG).

[0244] In some embodiments, the second adding step comprises adding about 1.0 mol% PEG lipid to the loaded LNP.

[0245] In some embodiments, after the second adding step, the loaded LNP solution (e.g., the loaded LNP) comprises about 1.0 mol%, about 1.1 mol%, about 1.2 mol%, about 1.3 mol%, about 1.4 mol%, about 1.5 mol%, about 1.6 mol%, about 1.7 mol%, about 1.8 mol%, about 1.9 mol%, about 2.0 mol%, about 2.1 mol%, about 2.2 mol%, about 2.3 mol%, about 2.4 mol%, about 2.5 mol%, about 2.6 mol%, about 2.7 mol%, about 2.8 mol%, about 2.9 mol%, about 3.0 mol%, about 3.1 mol%, about 3.2 mol%, about 3.3 mol%, about 3.4 mol%, about 3.5 mol%, about 3.6 mol%, about 3.7 mol%, about 3.8 mol%, about 3.9 mol%, about 4.0 mol%, about 4.1 mol%, about 4.2 mol%, about 4.3 mol%, about 4.4 mol%, about 4.5 mol%, about 4.6 mol%, about 4.7 mol%, about 4.8 mol%, about 4.9 mol%, or about 5.0 mol% of PEG lipid (e.g., PEG2k-DMG).Nucleic Acids Solution

[0246] In some embodiments, the nucleic acid solution comprises a nucleic acid in an aqueous buffer (e.g., ammonium sulfate, sodium bicarbonate, sodium citrate, sodium acetate, potassium phosphate, sodium phosphate, tri s(hydroxymethyl)aminom ethane (tris), HEPES, and the like).

[0247] In some embodiments, the nucleic acid solution comprises an acetate buffer.

[0248] In some embodiments, the nucleic acid solution comprises about 1 mM to about 200 mM acetate buffer, about 2 mM to about 180 mM acetate buffer, about 3 mM to about 160 mM acetate buffer, about 4 mM to about 150 mM acetate buffer, about 4 mM to about 140 mM acetate buffer, about 5 mM to about 130 mM acetate buffer, about 6 mM to about 120 mM acetate buffer, about 7 mM to about 110 mM acetate buffer, about 8 mM to about 100 mM acetate buffer, about 9 mM to about 90 mM acetate buffer, about 10 mM to about 80 mM acetate buffer, about 15 mM to about 70 mM acetate buffer, about 20 mM to about 60 mM acetate buffer, about 25 mM to about 50 mM acetate buffer, or about 30 mM to about 40 mM acetate buffer.

[0249] In some embodiments, the nucleic acid solution has a pH of 4.5±2.0, 4.5±1.5, 4.5±1.0, 4.5±0.9, 4.5±0.8, 4.5±0.7, 4.5±0.6, 4.5±0.5, 4.5±0.4, 4.5±0.3, 4.5±0.2, or 4.5±0.1.

[0250] In some embodiments, the nucleic acid solution comprises acetate buffer having a pH of about 3.5 to about 5.0.Loaded Lipid Nanoparticle Solution and Formulation (Loaded-LNP Solutions and Loaded- LNP Formulation)

[0251] In some embodiments, the methods of the present disclosure provide a loaded-LNP solution being prepared by a method disclosed herein.

[0252] In some embodiments, the methods of the present disclosure provide a loaded-LNP formulation being prepared by a method disclosed herein.

[0253] In some embodiments, the loaded-LNP solution comprises the loaded LNP. In some embodiments, the loaded-LNP solution comprises the loaded LNP at a concentration of greater than about 0.01 mg / mL, 0.05 mg / mL, 0.06 mg / mL, 0.07 mg / mL, 0.08 mg / mL, 0.09 mg / mL, 0.1 mg / mL, 0.15 mg / mL, 0.2 mg / mL, 0.3 mg / mL, 0.4 mg / mL, 0.5 mg / mL, 0.6 mg / mL, 0.7 mg / mL, 0.8 mg / mL, 0.9 mg / mL, or 1.0 mg / mL. In some embodiments, the loaded-LNP solution comprises the loaded LNP at a concentration ranging from about 0.01-1.0 mg / mL, 0.01-0.9 mg / mL, 0.01-0.8 mg / mL, 0.01-0.7 mg / mL, 0.01-0.6 mg / mL, 0.01-0.5 mg / mL, 0.01- 0.4 mg / mL, 0.01-0.3 mg / mL, 0.01-0.2 mg / mL, 0.01-0.1 mg / mL, 0.05-1.0 mg / mL, 0.05-0.9 mg / mL, 0.05-0.8 mg / mL, 0.05-0.7 mg / mL, 0.05-0.6 mg / mL, 0.05-0.5 mg / mL, 0.05-0.4 mg / mL, 0.05-0.3 mg / mL, 0.05-0.2 mg / mL, 0.05-0.1 mg / mL, 0.1-1.0 mg / mL, 0.2-0.9 mg / mL, 0.3-0.8 mg / mL, 0.4-0.7 mg / mL, or 0.5-0.6 mg / mL. In some embodiments, the loaded-LNP solution comprises a loaded LNP at a concentration up to about 5.0 mg / mL, 4.0 mg / mL, 3.0 mg / mL, 2.0 mg / mL, 1.0 mg / mL, 0.09 mg / mL, 0.08 mg / mL, 0.07 mg / mL, 0.06 mg / mL, or 0.05 mg / mL.

[0254] In some embodiments, the loaded-LNP solution comprises a loaded LNP in an aqueous buffer. In some embodiments, the loaded-LNP solution may further comprise a buffering agent and / or a salt. Exemplary suitable buffering agents include, but are not limited to, ammonium sulfate, sodium bicarbonate, sodium citrate, sodium acetate, potassium phosphate, sodium phosphate, HEPES, and the like. In some embodiments, the loaded-LNP solution comprises a buffering agent at a concentration ranging from about 0.1-100 mM, from about 0.5-90 mM, from about 1.0-80 mM, from about 2-70 mM, from about 3-60 mM, from about 4-50 mM, from about 5-40 mM, from about 6-30 mM, from about 7-20 mM, from about 8-15 mM, from about 9-12 mM. In some embodiments, the loaded-LNP solution comprises a buffering agent at a concentration of or greater than about 0.1 mM, 0.5 mM, 1 mM, 2 mM, 3 mM, 4 mM, 5 mM, 6 mM, 7 mM, 8 mM, 9 mM, 10 mM, 15 mM, 20 mM, 25 mM, 30 mM, 35 mM, 40 mM, 45 mM,or 50 mM. Exemplary suitable salts include, but are not limited to, potassium chloride, magnesium chloride, sodium chloride, and the like. In some embodiments, the loaded-LNP solution comprises a salt at a concentration ranging from about 1-500 mM, from about 5-400 mM, from about 10-350 mM, from about 15-300 mM, from about 20-250 mM, from about 30- 200 mM, from about 40-190 mM, from about 50-180 mM, from about 50-170 mM, from about 50-160 mM, from about 50-150 mM, or from about 50-100 mM. In some embodiments, the loaded-LNP solution comprises a salt at a concentration of or greater than about 1 mM, 5 mM, 10 mM, 20 mM, 30 mM, 40 mM, 50 mM, 60 mM, 70 mM, 80 mM, 90 mM, or 100 mM.

[0255] In some embodiments, the loaded-LNP solution may have a pH ranging from about 4.0 to about 8.5, from about 4.1 to about 8.4, from about 4.3 to about 8.2, from about 4.5 to about 8.0, about 4.6 to about 7.8, about 4.8 to about 7.6, about 5.0 to about 7.4, about 5.5 to about 7.2, about 6.0 to about 7.0, about 6.0 to about 6.9, about 6.0 to about 6.8, about 6.0 to about 6.7, about 6.0 to about 6.6, about 6.0 to about 6.5. In some embodiments, the second buffering agent may have a pH of or no greater than about 4.0, 4.1, 4.3, 4.5, 4.6, 4.7, 4.8, 4.9, 5.0, 5.2, 5.4, 5.6, 5.8, 6.0, 6.1, 6.2, 6.3, 6.4, 6.5, 6.6, 6.7, 6.8, 6.9, 7.0, 7.2, 7.4, 7.6, 7.8, 8.0, 8.2, 8.4, and 8.5

[0256] In some embodiments, the loaded-LNP solution has a pH in a range of about 3.0 to about 8.5, about about 3.5 to about 8.0, about 3.75 to about 7.5, about 4.0 to about 7.0, about 4.25 to about 6.5, about 4.5 to about 6.25, about 4.6 to about 6.0, about 4.8 to about 5.8, about 5.0 to about 5.75, about 5.0 to about 5.5.

[0257] In some embodiments, the loaded-LNP solution comprises about 5.0±2.0 mM, 5.0±1.5 mM, 5.0±1.0 mM, 5.0±0.9 mM, 5.0±0.8 mM, 5.0±0.7 mM, 5.0±0.6 mM, 5.0±0.5 mM, 5.0±0.4 mM, 5.0±0.3 mM, 5.0±0.2 mM, or 5.0±0.1 mM citrate, acetate, phosphate or tris.

[0258] In some embodiments, the loaded-LNP solution about 5.0±2.0 mM, 5.0±1.5 mM, 5.0±1.0 mM, 5.0±0.9 mM, 5.0±0.8 mM, 5.0±0.7 mM, 5.0±0.6 mM, 5.0±0.5 mM, 5.0±0.4 mM, 5.0±0.3 mM, 5.0±0.2 mM, or 5.0±0.1 mM acetate.

[0259] In some embodiments, the loaded-LNP solution may have a pH of 5.0±2.0, 5.0±1.5, 5.0±1.0, 5.0±0.9, 5.0±0.8, 5.0±0.7, 5.0±0.6, 5.0±0.5, 5.0±0.4, 5.0±0.3, 5.0±0.2, or 5.0±0.1.

[0260] In some embodiments, the loaded-LNP solution comprises acetate buffer having a pH of 5.0±2.0, 5.0±1.5, 5.0±1.0, 5.0±0.9, 5.0±0.8, 5.0±0.7, 5.0±0.6, 5.0±0.5, 5.0±0.4, 5.0±0.3, 5.0±0.2, or 5.0±0.1.

[0261] In some embodiments, the loaded-LNP solution comprises about 5 mM citrate, acetate, phosphate, or tris.

[0262] In some embodiments, the loaded-LNP solution comprises acetate.

[0263] In some embodiments, the loaded-LNP solution comprises about 5 mM acetate.

[0264] In some embodiments, the loaded-LNP solution comprises acetate having a pH of about 5.0.

[0265] In some embodiments, the loaded-LNP solution comprises about 5 mM acetate, wherein the aqueous buffer solution has a pH of about 5.0.

[0266] In some embodiments, the loaded-LNP solution comprises about phosphate buffer, wherein the phosphate buffer has a pH of about 8.0.

[0267] In some embodiments, the loaded-LNP solution comprises a phosphate.

[0268] In some embodiments, the loaded-LNP solution comprises a combination of acetate and phosphate buffer, wherein the phosphate buffer has a pH of about 5.0.

[0269] In some embodiments, the loaded-LNP solution comprises a combination of acetate and phosphate buffer.

[0270] In some embodiments, loaded-LNP solution further comprises a first organic solvent.

[0271] In some embodiments, the first organic solvent is an alcohol.

[0272] In some embodiments, the alcohol is ethanol.

[0273] In some embodiments, the loaded-LNP solution further comprises a tonicity agent.

[0274] In some embodiments, the loaded-LNP solution comprises a loaded LNP comprising from about 10 mg / mL to about 20 mg / mL ionizable lipid.

[0275] In some embodiments, the loaded-LNP solution comprises a loaded LNP comprising from about 10 mg / mL to about 20 mg / mL of IL-1.

[0276] In some embodiments, the loaded-LNP solution comprises a loaded LNP comprising from about 10 mg / mL to about 20 mg / mL of IL-2.

[0277] In some embodiments, the loaded-LNP solution comprises a loaded LNP comprising from about 4 mg / mL to about 8 mg / mL structural lipid.

[0278] In some embodiments, the loaded-LNP solution comprises a loaded LNP comprising from about 4 mg / mL to about 8 mg / mL of SL-2.

[0279] In some embodiments, the loaded-LNP solution comprises a loaded LNP comprising from about 2 mg / mL to about 5 mg / mL phospholipid.

[0280] In some embodiments, the loaded-LNP solution comprises a loaded LNP comprising from about 2 mg / mL to about 5 mg / mL of DSPC.

[0281] In some embodiments, the loaded-LNP solution comprises a loaded LNP comprising from about 0.1 mg / mL to about 1.0 mg / mL PEG lipid.

[0282] In some embodiments, the loaded-LNP solution comprises a loaded LNP comprising from about 0.1 mg / mL to about 1.0 mg / mL of PEG2k-DMG.

[0283] In some embodiments, the loaded-LNP solution comprises a loaded LNP comprising an ionizable lipid, a structural lipid, a phospholipid, and a PEG lipid.

[0284] In some embodiments, the loaded-LNP solution comprises a loaded LNP comprising IL-1, DSPC, SL-2, and PEG2k-DMG.

[0285] In some embodiments, the loaded-LNP solution comprises a loaded LNP comprising IL-2, DSPC, SL-2, and PEG2k-DMG.

[0286] In some embodiments, the loaded-LNP solution comprising a loaded LNP comprising less than about 2.5 mol % of a PEG lipid.

[0287] In some embodiments, the loaded-LNP solution comprising a loaded LNP comprising an ionizable lipid, a structural lipid, a phospholipid, and less than about 2.5 mol % of a PEG lipid.

[0288] n some embodiments, the loaded-LNP solution comprising a loaded LNP comprising from about 0.1 mol % to about 0.5 mol % of PEG2k-DMG.

[0289] In some aspects, the present disclosure provides a loaded-LNP solution comprising a loaded LNP comprising IL-1, SL-2, DSPC, and from about 0.1 mol % to about 0.5 mol % of PEG2k-DMG.

[0290] In some aspects, the present disclosure provides a loaded-LNP solution comprising a loaded LNP comprising IL-2, SL-2, DSPC, and from about 0.1 mol % to about 0.5 mol % of PEG2k-DMG.

[0291] In some embodiments, the loaded-LNP solution comprises a loaded LNP comprising:(a) from about 10 mg / mL to about 20 mg / mL of ionizable lipid;(b) from about 4 mg / mL to about 8 mg / mL of structural lipid;(c) from about 2 mg / mL to about 5 mg / mL of phospholipid; and(d) from about 0.1 mg / mL to about 1.0 mg / mL of PEG lipid.

[0292] In some embodiments, the loaded-LNP solution comprises a loaded LNP comprising a loaded LNP comprising:(a) about 15±10 mg / mL, about 15±9 mg / mL, about 15±8 mg / mL, about 15±7 mg / mL, about 15±6 mg / mL, about 15±5 mg / mL, about 15±4 mg / mL, about 15±3 mg / mL, or about 15±2 mg / mL of ionizable lipid;(b) about 6±4 mg / mL, about 6±3 mg / mL, about 6±2 mg / mL, or about 6±1 mg / mL of structural lipid;(c) about 3.0±1.0 mg / mL, about 3.0±0.9 mg / mL, about 3.0±0.8 mg / mL, about 3.0±0.7 mg / mL, about 3.0±0.6 mg / mL, about 3.0±0.5 mg / mL, about 3.0±0.4 mg / mL, about 3.0±0.3 mg / mL, about 3.0±0.2 mg / mL, or about 3.0±0.1 mg / mL of phospholipid; and(d) about 0.5±0.4 mg / mL, about 0.5±0.3 mg / mL, about 0.5±0.2 mg / mL, or about 0.5±0.1 mg / mL of PEG lipid.

[0293] In some embodiments, the loaded-LNP solution comprises a loaded LNP comprising:(a) from about 10 mg / mL to about 20 mg / mL ionizable lipid;(b) from about 4 mg / mL to about 8 mg / mL structural lipid;(c) from about 2 mg / mL to about 5 mg / mL phospholipid;(d) from about 0.1 mg / mL to about 1.0 mg / mL PEG lipid.

[0294] In some embodiments, the loaded-LNP solution comprises a loaded LNP comprising:(a) from about 10 mg / mL to about 20 mg / mL of IL-1;(b) from about 4 mg / mL to about 8 mg / mL of SL-2;(c) from about 2 mg / mL to about 5 mg / mL of DSPC; and(d) from about 0.1 mg / mL to about 1.0 mg / mL of PEG2k-DMG.

[0295] In some embodiments, the loaded-LNP solution comprises a loaded LNP comprising:(a) from about 10 mg / mL to about 20 mg / mL of IL-2;(b) from about 4 mg / mL to about 8 mg / mL of SL-2;(c) from about 2 mg / mL to about 5 mg / mL of DSPC; and(d) from about 0.1 mg / mL to about 1.0 mg / mL of PEG2k-DMG.

[0296] In some embodiments, the loaded-LNP solution comprises a loaded LNP comprising:(a) about 15±10 mg / mL, about 15±9 mg / mL, about 15±8 mg / mL, about 15±7 mg / mL, about 15±6 mg / mL, about 15±5 mg / mL, about 15±4 mg / mL, about 15±3 mg / mL, or about 15±2 mg / mL of IL-2;(b) about 6±4 mg / mL, about 6±3 mg / mL, about 6±2 mg / mL, or about 6±1 mg / mL of SL-2;(c) about 3.0±1.0 mg / mL, about 3.0±0.9 mg / mL, about 3.0±0.8 mg / mL, about 3.0±0.7 mg / mL, about 3.0±0.6 mg / mL, about 3.0±0.5 mg / mL, about 3.0±0.4 mg / mL, about 3.0±0.3 mg / mL, about 3.0±0.2 mg / mL, or about 3.0±0.1 mg / mL of DSPC; and(d) about 0.5±0.4 mg / mL, about 0.5±0.3 mg / mL, about 0.5±0.2 mg / mL, or about 0.5±0.1 mg / mL of PEG2k-DMG.

[0297] In some embodiments, the loaded-LNP solution comprises(a) a loaded LNP comprising:(i) ionizable lipid;(ii) structural lipid;(iii) phospholipid;(iv) PEG lipid; and(b) acetate buffer.

[0298] In some embodiments, the loaded-LNP solution comprises(a) a loaded LNP comprising:(i) from about 10 mg / mL to about 20 mg / mL of ionizable lipid;(ii) from about 4 mg / mL to about 8 mg / mL of structural lipid;(iii) from about 2 mg / mL to about 5 mg / mL of phospholipid;(iv) from about 0.1 mg / mL to about 1.0 mg / mL of PEG lipid; and(b) about 5 mM acetate buffer having a pH of about 5.2.

[0299] In some embodiments, the loaded-LNP solution comprises(a) a loaded LNP comprising:(i) from about 10 mg / mL to about 20 mg / mL of IL-2;(ii) from about 4 mg / mL to about 8 mg / mL of SL-2;(iii) from about 2 mg / mL to about 5 mg / mL of DSPC;(iv) from about 0.1 mg / mL to about 1.0 mg / mL of PEG2k-DMG; and(b) about 5 mM acetate buffer having a pH of about 5.2.

[0300] In some embodiments, the loaded-LNP solution comprises a loaded LNP having an average lipid nanoparticle diameter of about 200 nm or less, about 175 nm or less, about 150 nm or less, about 125 nm or less, about 100 nm or less, about 90 nm or less, about 80 nm or less, about 75 nm or less, about 70 nm or less, about 65 nm or less, about 60 nm or less, about 55 nm or less, about 50 nm or less, about 45 nm or less, about 40 nm or less, about 35 nm or less, about 30 nm or less, about 25 nm or less, or about 20 nm or less.

[0301] In some embodiments, the loaded-LNP solution comprises a loaded LNP having an average lipid nanoparticle diameter of about 15 nm to about 150 nm, about 20 nm to about 150 nm, about 25 nm to about 125 nm, about 30 nm to about 110 nm, about 35 nm to about 100 nm, about 40 nm to about 90 nm, about 45 nm to about 80 nm, or about 50 nm to about 70 nm.Loaded Lipid Nanoparticles (Loaded LNPs)

[0302] In some embodiments, the methods of the present disclosure provide a loaded LNP comprising an ionizable lipid, a structural lipid, and a phospholipid.

[0303] In some embodiments, the methods of the present disclosure provide an empty LNP comprising an ionizable lipid, a structural lipid, a phospholipid, and a phosphatidylserine phospholipid.

[0304] In some embodiments, the loaded LNPs comprises a PEG lipid.

[0305] In some embodiments, the loaded LNPs is free of PEG lipid.

[0306] In some embodiments, the loaded LNPs comprises from about 30 mol % to about 70 mol % of ionizable lipid.

[0307] In some embodiments, the loaded LNPs comprises from about 30 mol % to about 50 mol % of structural lipid.

[0308] In some embodiments, the loaded LNPs comprises from about 5 mol % to about 15 mol % of phospholipid lipid.

[0309] In some embodiments, the loaded LNPs comprises from about 0.1 mol % to about 1.0 mol % of PEG lipid.

[0310] In some embodiments, the loaded LNPs comprises from about 30 mol % to about 70 mol % of IL-1.

[0311] In some embodiments, the loaded LNPs comprises from about 30 mol % to about 70 mol % of IL-2.

[0312] In some embodiments, the loaded LNPs comprises from about 30 mol % to about 50 mol % of SL-2.

[0313] In some embodiments, the loaded LNPs comprises from about 5 mol % to about 15 mol % of DSPC.

[0314] In some embodiments, the loaded LNPs comprises from about 0.1 mol % to about 1.0 mol % of PEG2k-DMG.

[0315] In some embodiments, the loaded LNPs comprises:(a) from about 30 mol % to about 70 mol % of ionizable lipid;(b) from about 30 mol % to about 50 mol % of structural lipid;(c) from about 5 mol % to about 15 mol % of phospholipid; and(d) from about 0.1 mol % to about 1.0 mol % of PEG lipid.

[0316] In some embodiments, the loaded LNPs comprises:(a) IL-l;(b) SL-2;(c) DSPC; and(d) PEG2k-DMG.

[0317] In some embodiments, the loaded LNPs comprises:(a) IL-2;(b) SL-2;(c) DSPC; and(d) PEG2k-DMG.

[0318] In some embodiments, the loaded LNPs comprises:(a) from about 30 mol % to about 70 mol % of IL-1;(b) from about 30 mol % to about 50 mol % of SL-2;(c) from about 5 mol % to about 15 mol % of DSPC; and(d) from about 0.1 mol % to about 1.0 mol % of PEG2k-DMG.

[0319] In some embodiments, the loaded LNPs comprises:(a) from about 30 mol % to about 70 mol % of IL-2;(b) from about 30 mol % to about 50 mol % of SL-2;(c) from about 5 mol % to about 15 mol % of DSPC; and(d) from about 0.1 mol % to about 1.0 mol % of PEG2k-DMG.

[0320] In some embodiments, the loaded LNP comprises about 30-60 mol% IL-1; about 0-30 mol% DSPC; about 15-50 mol% SL-2; and about 0.1-0.5 mol% PEG2k-DMG. In some embodiments, the loaded LNP comprises about 0-30 mol% DSPC; about 15-50 mol% SL-2; and about 0.1-0.5 mol% PEG2k-DMG. In some embodiments, the loaded LNP comprises about 30-60 mol% IL-1; about 15-50 mol% SL-2; and about 0.1-0.5 mol% PEG2k-DMG. In some embodiments, the loaded LNP comprises about 30-60 mol% IL-1; about 0-30 mol% DSPC; and about 0.1-0.5 mol% PEG2k-DMG. In some embodiments, the loaded LNP comprises about 30-60 mol% IL-1; about 0-30 mol% DSPC; and about 15-50 mol% SL-2. In some embodiments, the loaded LNP comprises about 30-60 mol% IL-1 and about 0.1-0.5 mol% PEG2k-DMG. In some embodiments, the loaded LNP comprises about 30-60 mol% IL-1 and about 0-30 mol% DSPC. In some embodiments, the loaded LNP comprises about 30-60 mol% IL-1 and about 15-50 mol% SL-2. In some embodiments, the loaded LNP comprises about 0- 30 mol% DSPC and about 15-50 mol% SL-2. In some embodiments, the loaded LNP comprises about 0-30 mol% DSPC and about 0.1-0.5 mol% PEG2k-DMG. In some embodiments, the loaded LNP comprises about about 15-50 mol% SL-2 and about 0.1 -0.5 mol% PEG2k-DMG. In some embodiments, the loaded LNP comprises about 30-60 mol% IL- 1. In some embodiments, the loaded LNP comprises about 0-30 mol% DSPC. In some embodiments, the loaded LNP comprises about 15-50 mol% SL-2. In some embodiments, the loaded LNP comprises about 0.1-0.5 mol% PEG2k-DMG.

[0321] In some embodiments, the loaded LNP comprises about 30-60 mol% IL-2; about 0-30 mol% DSPC; about 15-50 mol% SL-2; and about 0.1-0.5 mol% PEG2k-DMG. In some embodiments, the loaded LNP comprises about 0-30 mol% DSPC; about 15-50 mol% SL-2; and about 0.1-0.5 mol% PEG2k-DMG. In some embodiments, the loaded LNP comprises about 30-60 mol% IL-2; about 15-50 mol% SL-2; and about 0.1-0.5 mol% PEG2k-DMG. In some embodiments, the loaded LNP comprises about 30-60 mol% IL-2; about 0-30 mol% DSPC;and about 0.1-0.5 mol% PEG2k-DMG. In some embodiments, the loaded LNP comprises about 30-60 mol% IL-2; about 0-30 mol% DSPC; and about 15-50 mol% SL-2. In some embodiments, the loaded LNP comprises about 30-60 mol% IL-2 and about 0.1-0.5 mol% PEG2k-DMG. In some embodiments, the loaded LNP comprises about 30-60 mol% IL-2 and about 0-30 mol% DSPC. In some embodiments, the loaded LNP comprises about 30-60 mol% IL-2 and about 15-50 mol% SL-2. In some embodiments, the loaded LNP comprises about 0- 30 mol% DSPC and about 15-50 mol% SL-2. In some embodiments, the loaded LNP comprises about 0-30 mol% DSPC and about 0.1-0.5 mol% PEG2k-DMG. In some embodiments, the loaded LNP comprises about about 15-50 mol% SL-2 and about 0.1 -0.5 mol% PEG2k-DMG. In some embodiments, the loaded LNP comprises about 30-60 mol% IL- 2. In some embodiments, the loaded LNP comprises about 0-30 mol% DSPC. In some embodiments, the loaded LNP comprises about 15-50 mol% SL-2. In some embodiments, the loaded LNP comprises about 0.1-0.5 mol% PEG2k-DMG.

[0322] In some embodiments, the loaded LNP comprises about 30-60 mol% IL-1; about 0-30 mol% DSPC; about 15-50 mol% SL-2; and about 0.1-10 mol% PEG2k-DMG. In some embodiments, the loaded LNP comprises about 0-30 mol% DSPC; about 15-50 mol% SL-2; and about 0.1-10 mol% PEG2k-DMG. In some embodiments, the loaded LNP comprises about 0-30 mol% DSPC; about 15-50 mol% SL-2; and about 0.1-10 mol% PEG2k-DMG. In some embodiments, the loaded LNP comprises about 30-60 mol% IL-1; about 15-50 mol% SL-2; and about 0.1-10 mol% PEG2k-DMG. In some embodiments, the loaded LNP comprises about 30-60 mol% IL-1; about 0-30 mol% DSPC; and about 0.1-10 mol% PEG2k-DMG. In some embodiments, the loaded LNP comprises about 30-60 mol% IL-1; about 0-30 mol% DSPC; and about 15-50 mol% SL-2. In some embodiments, the loaded LNP comprises about 30-60 mol% IL-1 and about 0-30 mol% DSPC. In some embodiments, the loaded LNP comprises about 30-60 mol% IL-1 and about 15-50 mol% SL-2. In some embodiments, the loaded LNP comprises about 30-60 mol% IL-1 and about 0.1-10 mol% PEG2k-DMG. In some embodiments, the loaded LNP comprises about 0-30 mol% DSPC and about 15-50 mol% SL- 2. In some embodiments, the loaded LNP comprises about 0-30 mol% DSPC about 0.1-10 mol% PEG2k-DMG. In some embodiments, the loaded LNP comprises about 15-50 mol% SL- 2 and about 0.1-10 mol% PEG2k-DMG. In some embodiments, the loaded LNP comprises about 30-60 mol% IL-1. In some embodiments, the loaded LNP comprises about 0-30 mol% DSPC. In some embodiments, the loaded LNP comprises about 15-50 mol% SL-2. In some embodiments, the loaded LNP comprises about 0. 1-10 mol% PEG2k-DMG.

[0323] In some embodiments, the loaded LNP comprises about 30-60 mol% IL-2; about 0-30 mol% DSPC; about 15-50 mol% SL-2; and about 0.1-10 mol% PEG2k-DMG. In some embodiments, the loaded LNP comprises about 0-30 mol% DSPC; about 15-50 mol% SL-2; and about 0.1-10 mol% PEG2k-DMG. In some embodiments, the loaded LNP comprises about 0-30 mol% DSPC; about 15-50 mol% SL-2; and about 0.1-10 mol% PEG2k-DMG. In some embodiments, the loaded LNP comprises about 30-60 mol% IL-2; about 15-50 mol% SL-2; and about 0.1-10 mol% PEG2k-DMG. In some embodiments, the loaded LNP comprises about 30-60 mol% IL-2; about 0-30 mol% DSPC; and about 0.1-10 mol% PEG2k-DMG. In some embodiments, the loaded LNP comprises about 30-60 mol% IL-2; about 0-30 mol% DSPC; and about 15-50 mol% SL-2. In some embodiments, the loaded LNP comprises about 30-60 mol% IL-2 and about 0-30 mol% DSPC. In some embodiments, the loaded LNP comprises about 30-60 mol% IL-2 and about 15-50 mol% SL-2. In some embodiments, the loaded LNP comprises about 30-60 mol% IL-2 and about 0.1-10 mol% PEG2k-DMG. In some embodiments, the loaded LNP comprises about 0-30 mol% DSPC and about 15-50 mol% SL- 2. In some embodiments, the loaded LNP comprises about 0-30 mol% DSPC about 0.1-10 mol% PEG2k-DMG. In some embodiments, the loaded LNP comprises about 15-50 mol% SL- 2 and about 0.1-10 mol% PEG2k-DMG. In some embodiments, the loaded LNP comprises about 30-60 mol% IL-2. In some embodiments, the loaded LNP comprises about 0-30 mol% DSPC. In some embodiments, the loaded LNP comprises about 15-50 mol% SL-2. In some embodiments, the loaded LNP comprises about 0. 1-10 mol% PEG2k-DMG.

[0324] In some embodiments, the population of loaded LNP has an average lipid nanoparticle diameter of about 200 nm or less, about 175 nm or less, about 150 nm or less, about 125 nm or less, about 100 nm or less, about 90 nm or less, about 80 nm or less, about 75 nm or less, about 70 nm or less, about 65 nm or less, about 60 nm or less, about 55 nm or less, about 50 nm or less, about 45 nm or less, about 40 nm or less, about 35 nm or less, about 30 nm or less, about 25 nm or less, or about 20 nm or less.

[0325] In some embodiments, the population of loaded LNP has an average lipid nanoparticle diameter of about 20 nm to about 150 nm, about 25 nm to about 125 nm, about 30 nm to about 110 nm, about 35 nm to about 100 nm, about 40 nm to about 90 nm, about 45 nm to about 80 nm, or about 50 nm to about 70 nm.Processing Steps

[0326] In some embodiments, the step of processing the empty-LNP solution or loaded-LNP solution further comprises at least one step selected from filtering, pH adjusting, bufferexchanging, diluting, dialyzing, concentrating, freezing, lyophilizing, storing, clarifying, adding cryoprotectant, filling, and packing.

[0327] In some embodiments, the step of processing the empty-LNP solution or loaded-LNP solution further comprises pH adjusting.

[0328] In some embodiments, the pH adjusting comprises adding a second buffering agent is selected from the group consisting of an acetate buffer, a citrate buffer, a phosphate buffer, and a tris buffer.

[0329] In some embodiments, the first adding step is performed prior to the pH adjusting.

[0330] In some embodiments, the first adding step is performed after the pH adjusting.

[0331] In some embodiments, the second adding step is performed prior to the pH adjusting.

[0332] In some embodiments, the second adding step is performed after the pH adjusting.

[0333] In some embodiments, the pH adjusting further comprises adding sucrose.

[0334] In some embodiments, the step of processing the intermediate empty-LNP solution, empty-LNP solution, or loaded-LNP solution further comprises filtering.

[0335] In some embodiments, the filtering is a tangential flow filtration (TFF).

[0336] In some embodiments, the filtering is a sterilizing or clarifying filtration.

[0337] In some embodiments, the filtering removes an organic solvent (e.g., an alcohol or ethanol) from the intermediate empty-LNP solution, empty-LNP solution, or loaded-LNP solution. In some embodiments, the filtering removes substantially all of the organic solvent (e.g., an alcohol or ethanol) from the intermediate empty-LNP solution, empty-LNP solution, or loaded-LNP solution. In some embodiments, the resulting LNP solution is sterilized before storage or use, e.g., by filtration (e.g., through a 0.1-0.5 pm filter).

[0338] In some embodiments, the step of processing the empty-LNP solution or loaded-LNP solution further comprises buffer exchanging.

[0339] In some embodiments, the buffer exchanging comprises addition of an aqueous buffer solution comprising a third buffering agent.

[0340] In some embodiments, the first adding step is performed prior to the buffer exchanging.

[0341] In some embodiments, the first adding step is performed after the buffer exchanging.

[0342] In some embodiments, the second adding is performed prior to the buffer exchanging.

[0343] In some embodiments, the second adding step is performed after the buffer exchanging.

[0344] In some embodiments, the step of processing the empty-LNP solution or loaded-LNP solution further comprises diluting.

[0345] In some embodiments, the step of processing the empty-LNP solution or loaded-LNP solution further comprises dialyzing.

[0346] In some embodiments, the step of processing the empty-LNP solution or loaded-LNP solution further comprises concentrating.

[0347] In some embodiments, the step of processing the empty-LNP solution or loaded-LNP solution further comprises freezing.

[0348] In some embodiments, the step of processing the empty-LNP solution or loaded-LNP solution further comprises lyophilizing.

[0349] In some embodiments, the lyophilizing comprises freezing the loaded-LNP solution at a temperature from about -100 °C to about 0 °C, about -80 °C to about -10 °C, about -60 °C to about -20 °C, about -50 °C to about -25 °C, or about -40 °C to about -30 °C.

[0350] In some embodiments, the lyophilizing further comprises drying the frozen loaded-LNP solution to form a lyophilized empty LNP or lyophilized loaded LNP.

[0351] In some embodiments, the drying is performed at a vacuum ranging from about 50 mTorr to about 150 mTorr.

[0352] In some embodiments, the drying is performed at about -35 °C to about -15 °C.

[0353] In some embodiments, the drying is performed at about room temperature to about 25 °C.

[0354] In some embodiments, the step of processing the empty-LNP solution or loaded-LNP solution further comprises storing.

[0355] In some embodiments, the step of processing the empty-LNP solution or loaded-LNP solution further comprises packing.

[0356] As used herein, “packing” may refer to storing a drug product in its final state or in- process storage of an empty LNP, loaded LNP, or LNP formulation before they are placed into final packaging. Modes of storage and / or packing include, but are not limited to, refrigeration in sterile bags, refrigerated or frozen formulations in vials, lyophilized formulations in vials and syringes, etc.

[0357] In some embodiments, the step of processing the empty-LNP solution or loaded-LNP solution comprises: iia) adding a cryoprotectant to the empty-LNP solution or loaded-LNP solution.

[0358] In some embodiments, the step of processing the empty-LNP solution or loaded-LNP solution comprises: iib) filtering the empty-LNP solution or loaded-LNP solution.

[0359] In some embodiments, the step of processing the empty-LNP solution or loaded-LNP solution comprises:

[0360] iia) adding a cryoprotectant to the empty-LNP solution or loaded-LNP solution; and

[0361] iic) filtering the empty-LNP solution or loaded-LNP solution.

[0362] In some embodiments, the step of processing the empty-LNP solution or loaded-LNP solution comprises one or more of the following steps: iib) adding a cryoprotectant to the empty-LNP solution or loaded-LNP solution; iic) lyophilizing the empty-LNP solution or loaded-LNP solution, thereby forming a lyophilized LNP composition; iid) storing the empty-LNP solution or loaded-LNP solution of the lyophilized LNP composition; and iie) adding a buffering solution to the empty-LNP solution, loaded-LNP solution, or the lyophilized LNP composition, thereby forming the empty-LNP formulation or loaded LNP formulation.

[0363] In some embodiments, the step of processing the empty-LNP solution comprises: iia) adding a cryoprotectant to the empty-LNP solution.

[0364] In some embodiments, the step of processing the empty-LNP solution comprises: iib) filtering the empty-LNP solution.

[0365] In some embodiments, the step of processing the empty-LNP solution comprises: iia) adding a cryoprotectant to the empty-LNP solution; and iic) filtering the empty-LNP solution.

[0366] Certain aspects of the methods are described in PCT Application No. WO / 2020 / 160397, which is incorporated herein by reference in their entirety.Adding a Cryoprotectant

[0367] In some embodiments, the step of processing the empty-LNP solution comprises: iia) adding a cryoprotectant to the empty-LNP solution.

[0368] In some embodiments, the step of processing the empty-LNP solution comprises: iib) filtering the empty-LNP solution.

[0369] In some embodiments, the step of processing the empty-LNP solution comprises: iia) adding a cryoprotectant to the empty-LNP solution; and iic) filtering the empty-LNP solution.

[0370] In some embodiments, the cryoprotectant is added to the empty-LNP solution or loaded-LNP solution prior to the lyophilization. In some embodiments, the cryoprotectant comprises one or more cryoprotective agents, and each of the one or more cryoprotective agents is independently a polyol (e.g., a diol or a triol such as propylene glycol (i.e., 1,2-propanediol), 1,3-propanediol, glycerol, (+ / -)-2-methyl-2,4-pentanediol, 1,6-hexanediol, 1,2-butanediol, 2,3- butanediol, ethylene glycol, or diethylene glycol), a nondetergent sulfobetaine (e.g., NDSB-201 (3 -(l-pyridino)-l -propane sulfonate), an osmolyte (e.g., L-proline or trimethylamine N- oxide dihydrate), a polymer (e.g., polyethylene glycol 200 (PEG 200), PEG 400, PEG 600, PEG 1000, PEG2k-DMG, PEG 3350, PEG 4000, PEG 8000, PEG 10000, PEG 20000, polyethylene glycol monomethyl ether 550 (mPEG 550), mPEG 600, mPEG 2000, mPEG 3350, mPEG 4000, mPEG 5000, polyvinylpyrrolidone (e.g., polyvinylpyrrolidone K 15), pentaerythritol propoxylate, or polypropylene glycol P 400), an organic solvent (e.g., dimethyl sulfoxide (DMSO) or ethanol), a sugar (e.g., D-(+)-sucrose, D-sorbitol, trehalose, D-(+)- maltose monohydrate, meso-erythritol, xylitol, myo-inositol, D-(+)-raffinose pentahydrate, D- (+)-trehalose dihydrate, or D-(+)-glucose monohydrate), or a salt (e.g., lithium acetate, lithium chloride, lithium formate, lithium nitrate, lithium sulfate, magnesium acetate, sodium acetate, sodium chloride, sodium formate, sodium malonate, sodium nitrate, sodium sulfate, or any hydrate thereof), or any combination thereof.

[0371] In some embodiments, the cryoprotectant comprises sucrose. In some embodiments, the cryoprotectant and / or excipient is sucrose. In some embodiments, the cryoprotectant comprises sodium acetate. In some embodiments, the cryoprotectant and / or excipient is sodium acetate. In some embodiments, the cryoprotectant comprises sucrose and sodium acetate.

[0372] In some embodiments, the cryoprotectant comprises a cryoprotective agent present at a concentration from about 10 g / L to about 1000 g / L, from about 25 g / L to about 950 g / L, from about 50 g / L to about 900 g / L, from about 75 g / L to about 850 g / L, from about 100 g / L to about 800 g / L, from about 150 g / L to about 750 g / L, from about 200 g / L to about 700 g / L, from about 250 g / L to about 650 g / L, from about 300 g / L to about 600 g / L, from about 350 g / L to about 550 g / L, from about 400 g / L to about 500 g / L, and from about 450 g / L to about 500 g / L. In some embodiments, the cryoprotectant comprises a cryoprotective agent present at a concentration from about 10 g / L to about 500 g / L, from about 50 g / L to about 450 g / L, from about 100 g / L to about 400 g / L, from about 150 g / L to about 350 g / L, from about 200 g / L to about 300 g / L, and from about 200 g / L to about 250 g / L. In some embodiments, the cryoprotectant comprises a cryoprotective agent present at a concentration of about 10 g / L, about 25 g / L, about 50 g / L, about 75 g / L, about 100 g / L, about 150 g / L, about 200 g / L, about 250 g / L, about 300 g / L, about 300 g / L, about 350 g / L, about 400 g / L, about 450 g / L, about 500 g / L, about 550 g / L, about 600 g / L, about 650 g / L, about 700 g / L, about 750 g / L, about 800 g / L, about 850 g / L, about 900 g / L, about 950 g / L, and about 1000 g / L.

[0373] In some embodiments, the cryoprotectant comprises a cryoprotective agent present at a concentration from about 0.1 mM to about 100 mM, from about 0.5 mM to about 90 mM, fromabout 1 mM to about 80 mM, from about 2 mM to about 70 mM, from about 3 mM to about 60 mM, from about 4 mM to about 50 mM, from about 5 mM to about 40 mM, from about 6 mM to about 30 mM, from about 7 mM to about 25 mM, from about 8 mM to about 20 mM, from about 9 mM to about 15 mM, and from about 10 mM to about 15 mM. In some embodiments, the cryoprotectant comprises a cryoprotective agent present at a concentration from about 0.1 mM to about 10 mM, from about 0.5 mM to about 9 mM, from about 1 mM to about 8 mM, from about 2 mM to about 7 mM, from about 3 mM to about 6 mM, and from about 4 mM to about 5 mM. In some embodiments, the cryoprotectant comprises a cryoprotective agent present at a concentration of about 0.1 mM, about 0.5 mM, about 1 mM, about 2 mM, about 3 mM, about 4 mM, about 5 mM, about 6 mM, about 7 mM, about 8 mM, about 9 mM, about 10 mM, about 15 mM, about 20 mM, about 25 mM, about 30 mM, about 35 mM, about 40 mM, about 45 mM, about 50 mM, about 55 mM, about 60 mM, about 65 mM, about 70 mM, about 75 mM, about 80 mM, about 85 mM, about 90 mM, about 95 mM, and about 100 mM.

[0374] In some embodiments, the cryoprotectant comprises an aqueous solution comprising sucrose.

[0375] In some embodiments, the cryoprotectant comprises an aqueous solution comprising about 700±300 g / L, 700±200 g / L, 700±100 g / L, 700±90 g / L, 700±80 g / L, 700±70 g / L, 700±60 g / L, 700±50 g / L, 700±40 g / L, 700±30 g / L, 700±20 g / L, 700±10 g / L, 700±9 g / L, 700±8 g / L, 700±7 g / L, 700±6 g / L, 700±5 g / L, 700±4 g / L, 700±3 g / L, 700±2 g / L, or 700±l g / L of sucrose.

[0376] In some embodiments, the cryoprotectant comprises an aqueous solution comprising about 200±100 g / L, 200±90 g / L, 200±80 g / L, 200±70 g / L, 200±60 g / L, 200±50 g / L, 200±40 g / L, 200±30 g / L, 200±20 g / L, 200±10 g / L, 200±9 g / L, 200±8 g / L, 200±7 g / L, 200±6 g / L, 200±5 g / L, 200±4 g / L, 200±3 g / L, 200±2 g / L, or 200±l g / L of sucrose.

[0377] In some embodiments, the cryoprotectant comprises an aqueous solution comprising sodium acetate and sucrose.

[0378] In some embodiments, the cryoprotectant comprises an aqueous solution comprising:(a) about 5±1 mM, about 5±0.9 mM, about 5±0.8 mM, about 5±0.5 mM, about 5±0.6 mM, about 5±0.5 mM, about 5±0.4 mM, about 5±0.3 mM, about 5±0.2 mM, or about 5±0.1 mM of sodium acetate; and(b) about 700±300 g / L, 700±200 g / L, 700±100 g / L, 700±90 g / L, 700±80 g / L, 700±70 g / L, 700±60 g / L, 700±50 g / L, 700±40 g / L, 700±30 g / L, 700±20 g / L, 700±10 g / L, 700±9 g / L, 700±8 g / L, 700±7 g / L, 700±6 g / L, 700±5 g / L, 700±4 g / L, 700±3 g / L, 700±2 g / L, or 700±l g / L of sucrose.

[0379] In some embodiments, the cryoprotectant comprises an aqueous solution comprising:(a) about 5±1 mM, about 5±0.9 mM, about 5±0.8 mM, about 5±0.5 mM, about 5±0.6 mM, about 5±0.5 mM, about 5±0.4 mM, about 5±0.3 mM, about 5±0.2 mM, or about 5±0.1 mM of sodium acetate; and(b) 200±100 g / L, 200±90 g / L, 200±80 g / L, 200±70 g / L, 200±60 g / L, 200±50 g / L, 200±40 g / L, 200±30 g / L, 200±20 g / L, 200±10 g / L, 200±9 g / L, 200±8 g / L, 200±7 g / L, 200±6 g / L, 200±5 g / L, 200±4 g / L, 200±3 g / L, 200±2 g / L, or 200±l g / L of sucrose.

[0380] In some embodiments, the cryoprotectant comprises an aqueous solution comprising sodium acetate and sucrose, wherein the aqueous solution has a pH value of 5.0±2.0, 5.0±1.5, 5.0±1.0, 5.0±0.9, 5.0±0.8, 5.0±0.7, 5.0±0.6, 5.0±0.5, 5.0±0.4, 5.0±0.3, 5.0±0.2, or 5.0±0.1.

[0381] In some embodiments, the cryoprotectant comprises an aqueous solution comprising:(a) about 5±1 mM, about 5±0.9 mM, about 5±0.8 mM, about 5±0.5 mM, about 5±0.6 mM, about 5±0.5 mM, about 5±0.4 mM, about 5±0.3 mM, about 5±0.2 mM, or about 5±0.1 mM of sodium acetate; and(b) about 700±300 g / L, 700±200 g / L, 700±100 g / L, 700±90 g / L, 700±80 g / L, 700±70 g / L, 700±60 g / L, 700±50 g / L, 700±40 g / L, 700±30 g / L, 700±20 g / L, 700±10 g / L, 700±9 g / L, 700±8 g / L, 700±7 g / L, 700±6 g / L, 700±5 g / L, 700±4 g / L, 700±3 g / L, 700±2 g / L, or 700±l g / L of sucrose; and wherein the aqueous solution has a pH value of 5.0±2.0, 5.0±1.5, 5.0±1.0, 5.0±0.9, 5.0±0.8, 5.0±0.7, 5.0±0.6, 5.0±0.5, 5.0±0.4, 5.0±0.3, 5.0±0.2, or 5.0±0.1.

[0382] In some embodiments, the cryoprotectant comprises an aqueous solution comprising:(a) about 5±1 mM, about 5±0.9 mM, about 5±0.8 mM, about 5±0.5 mM, about 5±0.6 mM, about 5±0.5 mM, about 5±0.4 mM, about 5±0.3 mM, about 5±0.2 mM, or about 5±0.1 mM of sodium acetate; and(b) 200±100 g / L, 200±90 g / L, 200±80 g / L, 200±70 g / L, 200±60 g / L, 200±50 g / L, 200±40 g / L, 200±30 g / L, 200±20 g / L, 200±10 g / L, 200±9 g / L, 200±8 g / L, 200±7 g / L, 200±6 g / L, 200±5 g / L, 200±4 g / L, 200±3 g / L, 200±2 g / L, or 200±l g / L of sucrose; and wherein the aqueous solution has a pH value of 5.0±2.0, 5.0±1.5, 5.0±1.0, 5.0±0.9, 5.0±0.8, 5.0±0.7, 5.0±0.6, 5.0±0.5, 5.0±0.4, 5.0±0.3, 5.0±0.2, or 5.0±0.1.

[0383] In some embodiments, the lyophilization is carried out in a suitable glass receptacle (e.g., a 10 mL cylindrical glass vial). In some embodiments, the glass receptacle can withstand extreme changes in temperatures between lower than -40 °C and higher than room temperature in short periods of time, and / or be cut in a uniform shape. In some embodiments, the step of lyophilizing comprises freezing the LNP solution at a temperature higher than about -40 °C,thereby forming a frozen LNP solution; and drying the frozen LNP solution to form the lyophilized LNP composition. In some embodiments, the step of lyophilizing comprises freezing the LNP solution at a temperature higher than about -40 °C and lower than about -30 °C. The freezing step results in a linear decrease in temperature to the final over about 6 minutes, preferably at about 1 °C per minute from 20 °C to -40 °C. In some embodiments, the freezing step results in a linear decrease in temperature to the final over about 6 minutes at about 1 °C per minute from 20 °C to -40 °C. In some embodiments, sucrose at 12-15% may be used, and the drying step is performed at a vacuum ranging from about 50 mTorr to about 150 mTorr. In some embodiments, sucrose at 12-15% may be used, and the drying step is performed at a vacuum ranging from about 50 mTorr to about 150 mTorr, first at a low temperature ranging from about -35 °C to about -15 °C, and then at a higher temperature ranging from room temperature to about 25 °C. In some embodiments, sucrose at 12-15% may be used, and the drying step is performed at a vacuum ranging from about 50 mTorr to about 150 mTorr, and the drying step is completed in three to seven days. In some embodiments, sucrose at 12-15% may be used, and the drying step is performed at a vacuum ranging from about 50 mTorr to about 150 mTorr, first at a low temperature ranging from about -35 °C to about -15 °C, and then at a higher temperature ranging from room temperature to about 25 °C, and the drying step is completed in three to seven days. In some embodiments, the drying step is performed at a vacuum ranging from about 50 mTorr to about 100 mTorr. In some embodiments, the drying step is performed at a vacuum ranging from about 50 mTorr to about 100 mTorr, first at a low temperature ranging from about -15 °C to about 0 °C, and then at a higher temperature.

[0384] In some embodiments, the empty-LNP solution, loaded-LNP solution, or the lyophilized LNP composition is stored at a pH from about 3.5 to about 8.0, from about 4.0 to about 7.5, from about 4.5 to about 7.0, from about 5.0 to about 6.5, and from about 5.5 to about 6.0. In some embodiments, the empty-LNP solution, loaded-LNP solution, or the lyophilized LNP composition is stored at a pH of about 3.5, about 4.0, about 4.5, about 4.6, about 4.7, about 4.8, about 4.9, about 5.0, about 5.1, about 5.2, about 5.3, about 5.4, about 4.5, about 5.5, about 6.5, about 7.0, about 7.5, and about 8.0.

[0385] In some embodiments, the LNP solution, loaded-LNP solution, or the lyophilized LNP composition is stored in a cryoprotectant comprising sucrose and sodium acetate. In some embodiments, the LNP solution, loaded-LNP solution, or the lyophilized LNP composition is stored in a cryoprotectant comprising from about 150 g / L to about 350 g / L sucrose and from about 3 mM to about 6 mM sodium acetate at a pH from about 4.5 to about 7.0. In someembodiments, the LNP solution, loaded-LNP solution, or the lyophilized LNP composition is stored in a cryoprotectant comprising about 200 g / L sucrose and 5 mM sodium acetate at about pH 5.0.

[0386] In some embodiments, the empty-LNP solution, loaded-LNP solution, or the lyophilized LNP composition is stored at a temperature of about -80 °C, about -78 °C, about - 76 °C, about -74 °C, about -72 °C, about -70 °C, about -65 °C, about -60 °C, about -55 °C, about -50 °C, about -45 °C, about -40 °C, about -35 °C, or about -30 °C prior to adding the buffering solution.

[0387] In some embodiments, the empty-LNP solution, loaded-LNP solution, or the lyophilized LNP composition is stored at a temperature of about -40 °C, about -35 °C, about - 30 °C, about -25 °C, about -20 °C, about -15 °C, about -10 °C, about -5 °C, about 0 °C, about 5 °C, about 10 °C, about 15 °C, about 20 °C, or about 25 °C prior to adding the buffering solution.

[0388] In some embodiments, the empty-LNP solution, loaded-LNP solution, or the lyophilized LNP composition is stored at a temperature of ranging from about -40 °C to about 0 °C, from about -35 °C to about -5 °C, from about -30 °C to about -10 °C, from about -25 °C to about -15 °C, from about -22 °C to about -18 °C, or from about -21 °C to about -19 °C prior to adding the buffering solution.

[0389] In some embodiments, the empty-LNP solution, loaded-LNP solution, or the lyophilized LNP composition is stored at a temperature of about -20 °C prior to adding the buffering solution.Phosphatidylserine Phospholipid

[0390] In some embodiments, the phosphatidylserine phospholipid is of Formula (PL-I): A Nfn(PL-I), or a salt thereof, wherein: n is 0, 1, 2, 3, 4, 5, 6, 7, 8, 9, or 10; m is O, 1, 2, 3, 4, 5, 6, 7, 8, 9, or 10;A is of the formula:each instance of L2is independently a bond or an optionally substituted Ci-6 alkylene,wherein one methylene unit of the optionally substituted Ci-6 alkylene is optionally replaced with -O-, -N(RN)-, -S-, -C(O)-, -C(O)N(RN)-, -NRNC(O)-, -C(O)O-, -OC(O)-, -OC(O)O-, -OC(O)N(RN)-, -NRNC(O)O-, or -NRNC(O)N(RN)-; each instance of R2is independently cholesterol, optionally substituted cycloalkyl, optionally substituted C1-30 alkyl, optionally substituted C1-30 alkenyl, or optionally substituted C1-30 alkynyl; optionally wherein one or more methylene units of the optionally substituted C1-30 alkyl, optionally substituted C1-30 alkenyl, or optionally substituted C1-30 alkynyl are independently replaced with optionally substituted carbocyclylene, optionally substituted heterocyclylene, optionally substituted arylene, optionally substituted heteroarylene, -N(RN)-, -O-, -S-, -C(O)-, -C(O)N(RN)-, -NRNC(O)-, -NRNC(O)N(RN)-, -C(O)O-, -OC(O)-, -OC(O)O-, -OC(O)N(RN)-, -NRNC(O)O-, -C(O)S-, -SC(O)-, -C(=NRN)-, -C(=NRN)N(RN)-, -NRNC(=NRN)-, -NRNC(=NRN)N(RN)-, -C(S)-, -C(S)N(RN)-, -NRNC(S)-, -NRNC(S)N(RN)-, -S(O)-, -OS(O)-, -S(O)O-, -OS(O)O-, -OS(O)2-, -S(O)2O-, -OS(O)2O-, -N(RN)S(O)-, -S(O)N(RN)-, -N(RN)S(O)N(RN)-, -OS(O)N(RN)-, -N(RN)S(O)O-, -S(O)2-, -N(RN)S(O)2-, -S(O)2N(RN)-, -N(RN)S(O)2N(RN)-, -OS(O)2N(RN)-, or -N(RN)S(O)2O-; each instance of RNis independently hydrogen, optionally substituted alkyl, or a nitrogen protecting group;Ring B is optionally substituted carbocyclyl, optionally substituted heterocyclyl, optionally substituted aryl, or optionally substituted heteroaryl; and p is 1 or 2.

[0391] In some embodiments, n of Formula PL-1 is 0. In some embodiments, m of Formula PL-1 is 1. In some embodiments, n of Formula PL-1 is 0 and m of Formula PL-1 is 1.

[0392] In some embodiments, the phosphatidylserine phospholipid is of Formula (PL-Ia):or a salt thereof. In some embodiments, n of Formula PL-Ia is 0. In some embodiments, m ofFormula PL-Ia is 1. In some embodiments, n of Formula PL-Ia is 0 and m of Formula PL-Ia is 1.

[0393] In some embodiments, the phosphatidylserine phospholipid is of Formula (PL-Ib):or a salt thereof.

[0394] In some embodiments, each instance of R2is independently C1-30, C9-21, Cn-19, or C13- 17 alkyl or C1-30, C9-21, Cn-19, or C13-17 alkenyl. In some embodiments, each instance of R2is independently Cn-19 alkyl. In some embodiments, each instance of R2is independently C13-17 alkyl. In some embodiments, one R2is C1-30, C9-21, Cn-19, or C 13-17 alkyl and a second R2is Ci- 30, C9-21, Cn-19, or C13-17 alkenyl. In some embodiments, one R2is C1-30 alkyl and a second R2is Ci-30 alkenyl. In some embodiments, one R2is Cn-19 alkyl and a second R2is Cn-19 alkenyl. In some embodiments, one R2is C13-17 alkyl and a second R2is C13-17 alkenyl. In some embodiments, each instance of R2is C13 alkyl. In some embodiments, each instance of R2is C17 alkyl. In some embodiments, each instance of R2is C17 alkenyl. In some embodiments, one instance of R2is C 17 alkyl and a second instance of R2is C 17 alkenyl.

[0395] In some embodiments, the phosphatidylserine phospholipid isor a salt of any of the foregoing.Ionizable Lipids

[0396] In some aspects, the ionizable lipid is of compound of Formula (IL- A):(IL-A) or its N-oxide, or a salt or isomer thereof, wherein:R1is selected from the group consisting of C5-30 alkyl, C5-20 alkenyl, -R*YR”, -YR”, and -R”M’R’;R2and R3are independently selected from the group consisting of H, C1-14 alkyl, C2-14 alkenyl, -R*YR”, -YR”, and -R*OR”, or R2and R3, together with the atom to which they are attached, form a heterocycle or carbocycle;R4is selected from the group consisting of hydrogen, a C3-6 carbocycle, -(CH2)nQ, -(CH2)nCHQR, -(CH2)oC(R12)2(CH2)n-oQ, -CHQR, -CQ(R)2, -C(O)NQR and unsubstituted Ci- 6 alkyl, where Q is selected from a carbocycle, heterocycle, -OR, -O(CH2)nN(R)2, -C(O)OR, -OC(O)R, -OC(O)O-, -CX3, -CX2H, -CXH2, -CN, -N(R)2, -C(O)N(R)2, -N(R)C(O)R, -N(R)S(O)2R, -N(R)C(O)N(R)2, -N(R)C(S)N(R)2, -N(R)R8, -N(R)S(O)2R8, -O(CH2)nOR, -N(R)C(=NR9)N(R)2, -N(R)C(=CHR9)N(R)2, -OC(O)N(R)2, -N(R)C(O)OR, -N(OR)C(O)R, -N(OR)S(O)2R, -N(OR)C(O)OR, -N(OR)C(O)N(R)2, -N(OR)C(S)N(R)2,N(OR)C(=NR9)N(R)2, -N(OR)C(=CHR9)N(R)2, -C(=NR9)N(R)2, -C(=NR9)R, -C(O)N(R)OR, -(CH2)nN(R)2and-C(R)N(R)2C(O)OR, NRAS(O)2RSX, and, wherein A is a 3-14 membered heterocycle containing one or more heteroatoms selected from N, O and S; and a is1, 2, 3, or 4; whereindenotes a point of attachment; each o is independently selected from 1, 2, 3, and 4, and each n is independently selected from 1, 2, 3, 4, and 5;R8is selected from the group consisting of C3-6 carbocycle and heterocycle;R9is selected from the group consisting of H, CN, NO2, C1-6 alkyl, -OR, -S(O)2R, - S(O)2N(R)2, C2-6 alkenyl, C3-6 carbocycle and heterocycle;R12is selected from the group consisting of H, OH, C1-3 alkyl, and C2-3 alkenyl; each R is independently selected from the group consisting of C1-6 alkyl, C1-3 alkyl-aryl, C2-3 alkenyl, and H;RAis selected from H and C1-3 alkyl;Rsxis selected from a C3-8 carbocycle, a 3-14 membered heterocycle containing one or more heteroatoms selected from N, O and S, C1-6 alkyl, C2-6 alkenyl, (C1-3 alkoxy)Ci-3 alkyl, (CH2)PIO(CH2)P2RSX1, and (CH2)PIRSX1, wherein the carbocycle and heterocycle are optionally substituted with one or more groups selected from oxo, C1-6 alkyl, and (C1-3 alkoxy)Ci-3 alkyl;RSX1is selected from C(O)NR14R14’, a C3-8 carbocycle, and a 3-14 membered heterocycle containing one or more heteroatoms selected from N, O and S, wherein the carbocycle and heterocycle are each optionally substituted with one or more groups selected from oxo, halo, C1-3 alkyl, (C1-3 alkoxy)Ci-3 alkyl, C1-6 alkylamino, di-(Ci-6 alkyl) amino, and NH2; each R13is selected from the group consisting of OH, oxo, halo, C1-6 alkyl, C1-6 alkoxy, C2-6 alkenyl, C1-6 alkylamino, di-(Ci-6 alkyl) amino, NH2, C(0)NH2, CN, and NO2;R14and R14are each independently selected from the group consisting of H and C1-6 alkyl; pi is selected from 1, 2, 3, 4, and 5;P2 is selected from 1, 2, 3, 4, and 5; each R5is independently selected from the group consisting of OH, C1-3 alkyl, C2-3 alkenyl, and H; each R6is independently selected from the group consisting of OH, C1-3 alkyl, C2-3 alkenyl, and H;R7is selected from the group consisting of C1-3 alkyl, C2-3 alkenyl, and H;M and M’ are independently selected from -C(O)O-, -OC(O)-, -OC(O)O-, -OC(O)-M”- C(O)O-,-C(O)N(RM)-, -N(RM)C(O)-, -C(O)-, -C(S)-, -C(S)S-, -SC(S)-, -CH(OH)-, -P(O)(O RM)O-, -S(O)2-, -S-S-, an aryl group, and a heteroaryl group, in which M” is a bond, C1-13 alkyl or C2- 13 alkenyl; each RMis independently selected from the group consisting of H, C1-6 alkyl and C2-6 alkenyl;each R’ is independently selected from the group consisting of C1-18 alkyl, C2-18 alkenyl, -R*YR”, -YR”, (CH2)qOR*, and H, and each q’ is independently selected from 1, 2, and 3; each R” is independently selected from the group consisting of C3-15 alkyl andC3-15 alkenyl; each R* is independently selected from the group consisting of C1-12 alkyl andC2-12 alkenyl; each Y is independently a C3-6 carbocycle; each X is independently selected from the group consisting of F, Cl, Br, and I; and m is selected from 5, 6, 7, 8, 9, 10, 11, 12, and 13.

[0397] In some aspects, the ionizable lipid is of compound of Formula (IL-B):r its N-oxide, or a salt or isomer thereof, wherein R’ais R’branched; whereinR’ branched jdenotes a point of attachment; wherein Raa, Rap, Raand Ra5are each independently selected from the group consisting of H, C2-12 alkyl, and C2-12 alkenyl;R2and R3are each independently selected from the group consisting of C1-14 alkyl andC2-14 alkenyl;R4is selected from the group consisting of -(CH2)nOH, wherein n is selected from the group consistingwhereindenotes a point of attachment; whereinR10is N(R)?; each R is independently selected from the group consisting of Ci-6 alkyl, C2-3 alkenyl, and H; and n2 is selected from the group consisting of 1, 2, 3, 4, 5, 6, 7, 8, 9, and 10; each R5is independently selected from the group consisting of C1-3 alkyl,C2-3 alkenyl, and H;each R6is independently selected from the group consisting of C1-3 alkyl, C2-3 alkenyl, and H;M and M’ are each independently selected from the group consisting of -C(O)O- and -OC(O)-;R’ is a C1-12 alkyl or C2-12 alkenyl;1 is selected from the group consisting of 1, 2, 3, 4, and 5; and m is selected from the group consisting of 5, 6, 7, 8, 9, 10, 11, 12, and 13.

[0398] In some aspects, the ionizable lipid is of compound a compound of Formula (IL-C):salt or isomer thereof, wherein1 is selected from 1, 2, 3, 4, and 5;Mi is M’;R4 is -(CH2)nQ, in which Q is OH, and n is selected from 1, 2, 3, 4, or 5;M and M’ are independently selected from -C(O)O- and -OC(O)-;R2 and R3 are both C1-14 alkyl, or C2-14 alkenyl; andR’ is a C1-C12 linear alkyl.

[0399] In some aspects, the ionizable lipid is of compound a compound of Formula (IL-D):wherein ? denotes a point of attachment; wherein Rayis selected from the group consisting of C1-12 alkyl and C2-12 alkenyl;R2and R3are each independently selected from the group consisting of C1-14 alkyl and C2-14 alkenyl;R4is -(CH2)nOH wherein n is selected from the group consisting of 1, 2, 3, 4, and 5;R’ is a C1-12 alkyl or C2-12 alkenyl;m is selected from 1, 2, 3, 4, 5, 6, 7, 8, and 9;1 is selected from 1, 2, 3, 4, 5, 6, 7, 8, and 9.

[0400] In some aspects, the ionizable lipid is a of compound of Formula (IL-I):r its N-oxide, or a salt or isomer thereof, wherein:R1is selected from the group consisting of C5-30 alkyl, C5-20 alkenyl, -R*YR”, -YR”, and -R”M’R’;R2and R3are independently selected from the group consisting of H, C1-14 alkyl, C2-14 alkenyl, -R*YR”, -YR”, and -R*OR”, or R2and R3, together with the atom to which they are attached, form a heterocycle or carbocycle;R4is selected from the group consisting of hydrogen, a C3-6 carbocycle, -(CH2)nQ, - (CH2)nCHQR, -(CH2)oC(R10)2(CH2)n-oQ, -CHQR, -CQ(R)2, and unsubstituted C1-6 alkyl, where Q is selected from a carbocycle, heterocycle, -OR, -O(CH2)nN(R)2, -C(O)OR, -OC(O)R, -CX3, -CX2H, -CXH2, -CN, -N(R)2, -C(O)N(R)2, -N(R)C(O)R, -N(R)S(O)2R, -N(R)C(O)N(R)2, - N(R)C(S)N(R)2, -N(R)R8, -N(R)S(O)2R8, -O(CH2)nOR,-N(R)C(=NR9)N(R)2, -N(R)C(=CHR9)N(R)2, -OC(O)N(R)2, -N(R)C(O)OR, -N(OR)C(O)R, -N(OR)S(O)2R, -N(OR)C(O)OR, -N(OR)C(O)N(R)2, -N(OR)C(S)N(R)2,-N(OR)C(=NR9)N(R)2, -N(OR)C(=CHR9)N(R)2, -C(=NR9)N(R)2, -C(=NR9)R,-C(O)N(R)OR, and -C(R)N(R)2C(O)OR, each o is independently selected from 1, 2, 3, and 4, and each n is independently selected from 1, 2, 3, 4, and 5; each R5is independently selected from the group consisting of OH, C1-3 alkyl, C2-3 alkenyl, and H; each R6is independently selected from the group consisting of OH, C1-3 alkyl, C2-3 alkenyl, and H;M and M’ are independently selected from -C(O)O-, -OC(O)-, -OC(O)-M”-C(O)O-, -C(O)N(R’)-, -N(R’)C(O)-, -C(O)-, -C(S)-, -C(S)S-, -SC(S)-, -CH(OH)-, -P(O)(OR’)O-, - S(O)2-, -S-S-, an aryl group, and a heteroaryl group, in which M” is a bond, C1-13 alkyl or C2- 13 alkenyl;R7is selected from the group consisting of C1-3 alkyl, C2-3 alkenyl, and H;R8is selected from the group consisting of C3-6 carbocycle and heterocycle;R9is selected from the group consisting of H, CN, NO2, C1-6 alkyl, -OR, -S(O)2R, - S(O)2N(R)2, C2-6 alkenyl, C3-6 carbocycle and heterocycle;R10is selected from the group consisting of H, OH, C1-3 alkyl, and C2-3 alkenyl; each R is independently selected from the group consisting of C1-3 alkyl, C2-3 alkenyl, (CH2)qOR*, and H, and each q is independently selected from 1, 2, and 3; each R’ is independently selected from the group consisting of C1-18 alkyl, C2-18 alkenyl, -R*YR”, -YR”, and H; each R” is independently selected from the group consisting of C3-15 alkyl andC3-15 alkenyl; each R* is independently selected from the group consisting of C1-12 alkyl andC2-12 alkenyl; each Y is independently a C3-6 carbocycle; each X is independently selected from the group consisting of F, Cl, Br, and I; and m is selected from 5, 6, 7, 8, 9, 10, 11, 12, and 13.

[0401] In some aspects, the ionizable lipid is a of compound of Formula (IL-IA):salt or isomer thereof, wherein1 is selected from 1, 2, 3, 4, and 5; m is selected from 5, 6, 7, 8, and 9;M1is a bond or M’;R4 is unsubstituted C1-3 alkyl, or -(CH2)nQ, in which Q isOH, -NHC(S)N(R)2, -NHC(O)N(R)2, -N(R)C(O)R, -N(R)S(O)2R, -N(R)R8,-NHC(=NR9)N(R)2, -NHC(=CHR9)N(R)2, -OC(O)N(R)2, -N(R)C(O)OR,-N(OR)C(O)R, -N(OR)S(O)2R, -N(OR)C(O)OR, -N(OR)C(O)N(R)2, -N(OR)C(S)N(R)2, -N(OR)C(=NR9)N(R)2, -N(OR)C(=CHR9)N(R)2, or heteroaryl, and each n is selected from 1,2, 3, 4, or 5;M and M’ are independently selected from -C(O)O-, -OC(O)-, -C(O)N(R’)-, -P(O)(OR’)O-, -S-S-, an aryl group, and a heteroaryl group; andR2 and R3 are both C1-14 alkyl or C2-14 alkenyl;Rs is selected from the group consisting of C3-6 carbocycle and heterocycle;R9 is selected from the group consisting of H, CN, NO2, C1-6 alkyl, -OR, -S(O)2R, -S(O)2N(R)2, C2-6 alkenyl, C3-6 carbocycle and heterocycle; each R is independently selected from the group consisting of C1-3 alkyl, C2-3 alkenyl, and H; andR’ is a Cuis alkyl or C2-18 alkenyl.

[0402] In some aspects, the ionizable lipid is a compound of Formula (IL-IB):or a salt or isomer thereof, wherein1 is selected from 1, 2, 3, 4, and 5; m is selected from 5, 6, 7, 8, and 9;R is selected from the group consisting of C1-14 alkyl and C2-14 alkenyl; andR2and R3are independently selected from the group consisting of C1-14 alkyl, and C2- 14 alkenyl;M and M’ are independently selected from -C(O)O- and -OC(O)-;RNis H, or C1-3 alkyl;Xaand Xbare each independently O or S;R10is selected from the group consisting of H, halo, -OH, R, -N(R)2, -CN, -N3, - C(O)OH, -C(O)OR, -OC(O)R, -OR, -SR, -S(O)R, -S(O)OR, -S(O)2OR, -NO2, -S(O)2N(R)2, - N(R)S(O)2R, -NH(CH2)tiN(R)2, -NH(CH2)piO(CH2)qiN(R)2, -NH(CH2)siOR, - N((CH2)SOR)2, -N(R)-carbocycle, -N(R)-heterocycle, -N(R)-aryl, -N(R)-heteroaryl, - N(R)(CH2)ti-carbocycle, -N(R)(CH2)ti-heterocycle, -N(R)(CH2)ti-aryl, -N(R)(CH2)ti- heteroaryl, a carbocycle, a heterocycle, aryl and heteroaryl; each R is independently selected from the group consisting of C1-12 alkyl, C2-12 alkenyl, and H; m is selected from 5, 6, 7, 8, 9, 10, 11, 12, and 13; n2 is selected from 1, 2, 3, 4, 5, 6, 7, 8, 9, and 10; r is 0 or 1; t1is selected from 1, 2, 3, 4, and 5; p1is selected from 1, 2, 3, 4, and 5; q1is selected from 1, 2, 3, 4, and 5; and s1is selected from 1, 2, 3, 4.

[0403] In some aspects, the ionizable lipid is a compound of Formula (IL-IC):whereindenotes a point of attachment; wherein Ray, Ray, and Rayare each C1-12 alkyl or C2-12 alkenyl;Rbyis H, C1-12 alkyl or C2-12 alkenyl;R2and R3are each independently selected from the group consisting of C1-14 alkyl and C2-14 alkenyl;R4is -(CH2)n0H;denotes a point of attachment; each R’ independently is a C1-12 alkyl or C2-12 alkenyl;R10is N(R)2; each R is independently selected from the group consisting of C1-6 alkyl, C2-3 alkenyl, and H; and n and n2 are each selected from the group consisting of 1, 2, 3, 4, and 5;Yais a C3-6 carbocycle;R*”ais selected from the group consisting of C1-15 alkyl and C2-15 alkenyl;1 is selected from 1, 2, 3, 4, and 5; m is selected from 5, 6, 7, 8, and 9; and s is 2 or 3.

[0404] In some embodiments, the ionizable lipid is a compound of Formula (IL*)or a salt thereof, wherein:R1is -OH, -NRN-C4-10 cycloalkenyl optionally substituted with one or more oxo or - N(RN’RN”);RNis H or C1-6 alkyl;RNis H or C1-6 alkyl;RNis H or C1-6 alkyl; o is 1, 2, 3, or 4; n is 4, 5, 6, 7, or 8; m is 4, 5, 6, 7, or 8;M is -C(=O)-O-* or -O-C(=O)-*, wherein * indicates attachment to R2;M’ is -C(=O)-O-* or -O-C(=O)-*, wherein * indicates attachment to R3;R2aR2bor -(Ci-6 alkylene)-(C3-8 cycloalkyl)-Ci-6 alkyl;R2ais -H or Ci-io alkyl;R2bis -H or Ci-io alkyl;R2Cis C I-8 alkyl or C2-8 alkenyl;R3ais H or Ci-10 alkyl;R3bis H or C 1-8 alkyl; andR3Cis Ci-10 alkyl or C2-8 alkenyl.

[0405] In some embodiments, the ionizable lipid is of Formula (IL**-I):(IL** -I) or a salt thereof, wherein:R1is -OH; o is 2, 3, or 4; n is 4, 5, 6, 7, or 8;M is -C(=O)-O-*, wherein * indicates attachment to R2; m is 6, 7, or 8;M’ is -C(=O)-O-*, wherein * indicates attachment to R3;R2Cis C4-8 alkyl;R3ais C7-10 alkyl; andR3Cis C3-5 alkyl.

[0406] In some embodiments, the ionizable lipid is of Formula (IL**-III):(IL**-III) or a salt thereof, wherein:R1is NRN-C4-10 cycloalkenyl optionally substituted with one or more oxo or -N(RN’RN”);RNis H;RNis C 1-2 alkyl;RN” is H; o is 2, 3, or 4; n is 6, 7, or 8;M is -C(=O)-O-*, wherein * indicates attachment to R2; m is 6, 7, or 8;M’ is -C(=O)-O-*, wherein * indicates attachment to R3;R2ais C7-10 alkyl;R2Cis C4-6 alkyl;R3ais C 1-3 alkyl; andR3Cis C4-6 alkyl.

[0407] In some embodiments, the ionizable lipid is of Formula (IL**-IV):(IL** -IV) or a salt thereof, wherein:R1is OH; o is 2, 3, or 4; n is 6, 7, or 8;M is -C(=O)-O-*, wherein * indicates attachment to R2; m is 6, 7, or 8;M’ is -C(=O)-O-*, wherein * indicates attachment to R3;R2bis C3-5 alkyl;R2Cis C2-4 alkyl;R3ais C7-10 alkyl; andR3Cis C4-6 alkyl.

[0408] In some embodiments, the ionizable lipid is of Formula (IL*-I):(IL*-Ia) or a salt thereof, wherein:R1, o, m, n, M, M’, R2c, and R3care as defined for variable IL*; andR3ais C i-8 alkyl.

[0409] In some embodiments, ionizable lipid is of Formula (IL*-Ia):or a salt thereof, wherein:R1, o, m, n, M, M’, R2c, and R3care as defined for Formula IL*; and R3ais C 1-8 alkyl.

[0410] In some embodiments, the ionizable lipid is of Formula (IL*-Ia’):or a salt thereof, wherein: o, M, M’, R2Cand R3care as defined for variable IL*; and R3ais C i-8 alkyl.

[0411] In some embodiments, the ionizable lipid is of Formula (IL*-IIa):or a salt thereof, wherein:R1, o, m, n, M, M’, R2c, and R3care as defined for Formula IL*; and R3ais C i-8 alkyl.

[0412] In some embodiments, the ionizable lipid is of Formula (IL*-II’):or a salt thereof, wherein: o, M, M’, R2Cand R3care as defined for variable IL*; and R3ais C i-8 alkyl.

[0413] In some embodiments, the ionizable lipid is of Formula (IL*-III):or a salt thereof, wherein:R1, o, m, n, M, M’, R2c, and R3care as defined for variable IL*;R2ais a C 1-8 alkyl; andR3ais C 1-8 alkyl.

[0414] In some embodiments, the ionizable lipid is of Formula (IL*-IIIa):or a salt thereof, wherein:R1, o, m, n, M, M’, R2c, and R3care as defined for variable IL*;R2bis a C i-8 alkyl; andR3ais C i-8 alkyl.

[0415] In some embodiments, the ionizable lipid is of Formula (IL*-IIIa):or a salt thereof, wherein:R1, o, M, M’, R2C, and R3care as defined for variable IL*;R2ais a C i-8 alkyl; andR3ais C i-8 alkyl.

[0416] In some embodiments, the ionizable lipid is of Formula (IL*-IIIa’):(IL*-IIIa’) or a salt thereof, wherein:R1, o, M, M’, R2C, and R3care as defined for variable IL*;R2ais a C i-8 alkyl; andR3ais C i-8 alkyl.

[0417] In some embodiments, the ionizable lipid is of Formula (IL*-IIIb):(IL*-IIIb) or a salt thereof, wherein:R1, o, M, M’, R2C, and R3care as defined for variable IL*;R2ais a C 1-8 alkyl; andR3ais C i-8 alkyl.

[0418] In some embodiments, the ionizable lipid is of Formula (IL*-IIIb’):(IL*-IIIb’) or a salt thereof, wherein:R1, o, M, M’, R2C, and R3care as defined for variable IL*;R2ais a C 1-8 alkyl; andR3ais C 1-8 alkyl.

[0419] In some embodiments, the ionizable lipid is of Formula (IL*-IV):(IL*-IV) or a salt thereof, wherein:R1, o, m, n, M, M’, R2c, and R3care as defined for variable IL*;R2bis a C i-8 alkyl; andR3ais C i-8 alkyl.

[0420] In some embodiments, the ionizable lipid is of Formula (IL*-IVa):or a salt thereof, wherein:R1, o, m, n, M, M’, R2c, and R3care as defined for variable IL*;R2bis a C i-8 alkyl; andR3ais C i-8 alkyl.

[0421] In some embodiments, the ionizable lipid is of Formula (IL*-Iva’):(ILMVa) or a salt thereof, wherein: o, M, M’, R2C, and R3care as defined for variable IL*;R2ais a C 1-8 alkyl; andR3ais C 1-8 alkyl.Variables o, R1, R RN, RNof Ionizable Lipid

[0422] In some embodiments of the ionizable lipid, o is 1.

[0423] In some embodiments of the ionizable lipid, o is 2.

[0424] In some embodiments of the ionizable lipid, o is 3.

[0425] In some embodiments of the ionizable lipid, o is 4.

[0426] In some embodiments of the ionizable lipid, R1is -OH.

[0427] In some embodiments of the ionizable lipid, RNis H.

[0428] In some embodiments of the ionizable lipid, RNis methyl.

[0429] In some embodiments of the ionizable lipid, RNis ethyl.

[0430] In some embodiments of the ionizable lipid, R1is -NRN-cyclobutenyl, wherein the cyclobutenyl is optionally substituted with one or more oxo or -N(RNRN”).

[0431] In some embodiments of the ionizable lipid, RNis H.

[0432] In some embodiments of the ionizable lipid, RNis methyl.

[0433] In some embodiments of the ionizable lipid, RNis ethyl.

[0434] In some embodiments of the ionizable lipid, RNis H.

[0435] In some embodiments of the ionizable lipid, RNis methyl.

[0436] In some embodiments of the ionizable lipid, RNis ethyl.

[0437] In some embodiments of the ionizable lipid, RNis H and RNis methyl.

[0438] In some embodiments of the ionizable lipid,

[0439] In some embodiments of the ionizable lipid,Variables m and n of the Ionizable Lipid

[0440] In some embodiments of the ionizable lipid, m is 4.

[0441] In some embodiments of the ionizable lipid, m is 5.

[0442] In some embodiments of the ionizable lipid, m is 6.

[0443] In some embodiments of the ionizable lipid, m is 7.

[0444] In some embodiments of the ionizable lipid, m is 8.

[0445] In some embodiments of the ionizable lipid, m is 4.

[0446] In some embodiments of the ionizable lipid, n is 5.

[0447] In some embodiments of the ionizable lipid, n is 6.

[0448] In some embodiments of the ionizable lipid, n is 7.

[0449] In some embodiments of the ionizable lipid, n is 8.

[0450] In some embodiments of the ionizable lipid, n is 5 and m is 7.

[0451] In some embodiments of the ionizable lipid, n is 7 and m is 7.

[0452] In some embodiments of the ionizable lipid, m is 6 and n is 6.Variables M and M ’

[0453] In some embodiments of the ionizable lipid, M is -O-C(=O)-*, wherein * indicates attachment to R2.

[0454] In some embodiments of the ionizable lipid, M is -C(=O)-O-* wherein * indicates attachment to R2.

[0455] In some embodiments of the ionizable lipid, M’ is -O-C(=O)-*, wherein * indicates attachment to R3.

[0456] In some embodiments of the ionizable lipid, M’ is -C(=O)-O-* wherein * indicates attachment to R3.

[0457] In some embodiments of the ionizable lipid, M is -O-C(=O)-* , wherein * indicates attachment to R2, and M’ is -C(=O)-O-* wherein * indicates attachment to R3Variables R2, R2a, R2b, R2cR2aR2b

[0458] In some embodiments of the ionizable lipid, R2is

[0459] In some embodiments of the ionizable lipid, R2ais hydrogen.

[0460] In some embodiments of the ionizable lipid, R2ais methyl.

[0461] In some embodiments of the ionizable lipid, R2ais ethyl.

[0462] In some embodiments of the ionizable lipid, R2ais propyl.

[0463] In some embodiments of the ionizable lipid, R2ais butyl.

[0464] In some embodiments of the ionizable lipid, R2ais pentyl.

[0465] In some embodiments of the ionizable lipid, R2ais hexyl.

[0466] In some embodiments of the ionizable lipid, R2ais heptyl.

[0467] In some embodiments of the ionizable lipid, R2ais octyl.

[0468] In some embodiments of the ionizable lipid, R2bis hydrogen.

[0469] In some embodiments of the ionizable lipid, R2bis methyl.

[0470] In some embodiments of the ionizable lipid, R2bis ethyl.

[0471] In some embodiments of the ionizable lipid, R2bis propyl.

[0472] In some embodiments of the ionizable lipid, R2bis butyl.

[0473] In some embodiments of the ionizable lipid, R2bis pentyl.

[0474] In some embodiments of the ionizable lipid, R2bis hexyl.

[0475] In some embodiments of the ionizable lipid, R2bis heptyl.

[0476] In some embodiments of the ionizable lipid, R2bis octyl.

[0477] In some embodiments of the ionizable lipid, R2ais hydrogen and R2bis hydrogen.

[0478] In some embodiments of the ionizable lipid, R2ais hexyl and R2bis hydrogen.

[0479] In some embodiments of the ionizable lipid, R2ais octyl and R2bis hydrogen.

[0480] In some embodiments of the ionizable lipid, R2ais hydrogen and R2bis butyl.

[0481] In some embodiments of the ionizable lipid, R2cis methyl.

[0482] In some embodiments of the ionizable lipid, R2cis ethyl.

[0483] In some embodiments of the ionizable lipid, R2cis propyl.

[0484] In some embodiments of the ionizable lipid, R2cis butyl.

[0485] In some embodiments of the ionizable lipid, R2cis pentyl.

[0486] In some embodiments of the ionizable lipid, R2cis hexyl.

[0487] In some embodiments of the ionizable lipid, R2cis heptyl.

[0488] In some embodiments of the ionizable lipid, R2cis octyl.

[0489] In some embodiments of the ionizable lipid, R2is -(Ci-6 alkylene)-(C3-8 cycloalkyl)-Ci- 6 alkyl.

[0490] In some embodiments of the ionizable lipid, R2is -(Ci-6 alkylene)-(cyclohexyl)-Ci-6 alkyl.

[0491] In some embodiments of the ionizable lipid, R2is -(Ci-6 alkylene)-(cyclopentyl)-Ci-6 alkyl.Variables R3, R3a, R3b, andR3c

[0492] In some embodiments of the ionizable lipid, R3

[0493] In some embodiments of the ionizable lipid, R3ais hydrogen.

[0494] In some embodiments of the ionizable lipid, R3ais methyl.

[0495] In some embodiments of the ionizable lipid, R3ais ethyl.

[0496] In some embodiments of the ionizable lipid, R3ais propyl.

[0497] In some embodiments of the ionizable lipid, R3ais butyl.

[0498] In some embodiments of the ionizable lipid, R3ais pentyl.

[0499] In some embodiments of the ionizable lipid, R3ais hexyl.

[0500] In some embodiments of the ionizable lipid, R3ais heptyl.

[0501] In some embodiments of the ionizable lipid, R3ais octyl.

[0502] In some embodiments of the ionizable lipid, R3bis hydrogen.

[0503] In some embodiments of the ionizable lipid, R3bis methyl.

[0504] In some embodiments of the ionizable lipid, R3bis ethyl.

[0505] In some embodiments of the ionizable lipid, R3bis propyl.

[0506] In some embodiments of the ionizable lipid, R3bis butyl.

[0507] In some embodiments of the ionizable lipid, R3bis pentyl.

[0508] In some embodiments of the ionizable lipid, R3bis hexyl.

[0509] In some embodiments of the ionizable lipid, R3bis heptyl.

[0510] In some embodiments of the ionizable lipid, R3bis octyl.

[0511] In some embodiments of the ionizable lipid, R3ais octyl and R3bis hydrogen.

[0512] In some embodiments of the ionizable lipid, R3ais ethyl and R3bis hydrogen.

[0513] In some embodiments of the ionizable lipid, R3ais hexyl and R3bis hydrogen.

[0514] In some embodiments of the ionizable lipid, R3cis methyl.

[0515] In some embodiments of the ionizable lipid, R3cis ethyl.

[0516] In some embodiments of the ionizable lipid, R3cis propyl.

[0517] In some embodiments of the ionizable lipid, R3cis butyl.

[0518] In some embodiments of the ionizable lipid, R3cis pentyl.

[0519] In some embodiments of the ionizable lipid, R3cis hexyl.

[0520] In some embodiments of the ionizable lipid, R3cis heptyl.

[0521] In some embodiments of the ionizable lipid, R3cis octyl.It is understood that, for an ionizable lipid, variables o, R1, RN, RN, RN, m, n, M, M’, R2, R2a, R2b, R2C, R3, R3a, R3b, and R3ccan each be, where applicable, selected from the groups described herein, and any group described herein for any of variables o,.R RN, RN, RN, m, n, M, M’, R2, R2a, R2b, R2C, R3, R3a, R3b, and R3ccan be combined, where applicable, with any group described herein for one or more of the remainder of variables o, R1, RN, RN, RN, m, n, M, M’, R2, R2a, R2b, R2C, R3, R3a, R3b, and R3c.

[0522] In some embodiments, the ionizable lipid is a compound selected from Table IL-1.Table IL-1: Ionizable lipids

[0523] In some embodiments, the ionizable lipid is a compound selected from Table IL-2.Table IL-2: Ionizable lipids

[0524] In some aspects, the ionizable lipid is a compound of Formula (IL-IIA):(IL-IIA), or its N-oxide, or a salt or isomer thereof, wherein: m is selected from 5, 6, 7, 8, and 9;R2and R3are each independently selected from the group consisting of H, C1-14 alkyl, and C2-14 alkenyl;R4is selected from -(CH2)nOH, wherein n is selected from 1, 2, 3, 4, and 5, and, wherein n2 is selected from 1, 2, 3, 4, 5, 6, 7, 8, 9, and 10; and R10is - N(R)2, wherein each R is independently selected from the group consisting of Ci-6 alkyl, C2-3 alkenyl, and H;M is selected from -OC(O)O-, -C(O)O-, -O-M”-O-, and -N(RM)C(O)-, in which M” is -(CH2)ZC(O)-, wherein z is 1, 2, 3, or 4;M’ is selected from -OC(O)O-, -C(O)O-, -O-M”-O-, -N(RM)C(O)O-, and -O- N=C(RM)-, wherein:M” is -(CH2)ZC(O)-, Ci-13 alkyl, -B(R**)-, or -Si(R**)2-;z is 1, 2, 3, or 4; each RMis independently selected from H and C1-6 alkyl; each R** is independently selected from H and C1-12 alkyl;R’ais Cuis alkyl, C2-18 alkenyl, or -R*YR*”, wherein: each R*” is independently C1-15 alkyl; each R* is independently C1-12 alkyl; each Y is independently a C3-6 carbocycle; and R” is a C3-C13 alkyl, optionally substituted with OH.

[0525] In some aspects, the ionizable lipid is a compound of Formula (IL-IIAX):r its N-oxide, or a salt or isomer thereof, wherein:R1is -R”M’R’, wherein: each R’ is independently Cuis alkyl;M’ is selected from -C(O)O- and -O-N=C(RM)-, wherein each RMis independently selected from H and C1-6 alkyl; each R” is independently C3-15 alkyl;R2and R3are each independently selected from the group consisting of H, C1-14 alkyl, and C2-14 alkenyl;R4is selected from -(CH2)nOH, wherein n is selected from 1, 2, 3, 4, and 5, and, wherein n2 is selected from 1, 2, 3, 4, 5, 6, 7, 8, 9, and 10; and R10is - N(R)2, wherein each R is independently selected from the group consisting of C1-6 alkyl, C2-3 alkenyl, and H; each R5is H; each R6is H; and m is selected from 5, 6, 7, 8, 9, 10, 11, 12, and 13.

[0526] In some embodiments, the ionizable lipid is a compound selected from Table IL-3.Table IL-3: Ionizable lipids

[0527] In some aspects, the ionizable lipid is a compound of Formula (IL-IIB):whereindenotes a point of attachment;Rap, Ray, and Ra5are each independently selected from the group consisting of H,Ci-12 alkyl, and C2-12 alkenyl;Rbp, Rby, and Rb5are each independently selected from the group consisting of H, C1-12 alkyl, and C2-12 alkenyl, wherein at least one of Rbp, Rby, and Rb5is selected from the group consisting of C1-12 alkyl and C2-12 alkenyl;R2and R3are each independently selected from the group consisting of C1-14 alkyl andC2-14 alkenyl;R4is selected from -(CH2)nNRTQ, -(CH2)nNRS(O)2TQ, -(CH2)nNRC(O)H and -(CH2)nNRC(O)TQ wherein n is selected from 1, 2, 3, 4, and 5;T is a bond or a C1-3 alkyl linker, C2-3 alkenyl linker, or C2-3 alkynyl linker;Q is selected from 3-14 membered heterocycle containing 1-5 heteroatoms selected from N, O, and S, C3-10 carbocycle, C1-6 alkyl, and C2-6 alkenyl, wherein the alkyl, alkenyl, heterocycle, and carbocycle are each optionally substituted with one or more RQ; each RQindependently is selected from the group consisting of oxo, hydroxyl, cyano, amino, C1-6 alkylamino, di-Ci-6 alkylamino, C1-6 alkyl, C1-6 alkoxy, C2-6 alkenyl, C1-6 alkanolyl, -C(O)Ci-6 alkyl, and -NRC(0)CI-6 alkyl; each R is independently selected from H, C1-6 alkyl, and C2-6 alkenyl; each R’ is independently selected from C1-12 alkyl and C2-12 alkenyl; m is selected from 1, 2, 3, 4, 5, 6, 7, 8, and 9; and1 is selected from 1, 2, 3, 4, 5, 6, 7, 8, and 9.

[0528] In some embodiments, the ionizable lipid is a compound selected from Table IL-4.

[0529] In some embodiments, the ionizable lipid is a compound selected from Table IL-5.Table IL-5: Ionizable lipids

[0530] In some aspects, the ionizable lipid is a compound of Formula (IL-IIC):r its N-oxide, or a salt or isomer thereof, wherein:R’ branched idenotes a point of attachment; wherein Raaand Rapare each independently selected from the group consisting of H and Ci-2 alkyl, wherein at least one of Raaand Rapis a Ci or C2 alkyl;R’ is selected from the group consisting of Cuis alkyl and C2-18 alkenyl;R2and R3are each independently selected from the group consisting of C1-14 alkyl and C2-14 alkenyl;R4is -(CH2)nQ, wherein n is independently selected from 1, 2, 3, 4, and 5, where Q is selected fromwherein A is a 3-14 membered heterocycle containing one or more heteroatoms selected from N, O and S; and a is 1, 2, 3, or4; wherein denotes a point of attachment;R is selected from H and C1-3 alkyl;Rsxis selected from a C3-8 carbocycle, a 3-14 membered heterocycle containing one or more heteroatoms selected from N, O and S, C1-6 alkyl, C2-6 alkenyl, (C1-3 alkoxy)Ci-3 alkyl, (CH2)PIO(CH2)P2RSX1, and (CH2)PIRSX1, wherein the carbocycle and heterocycle are optionally substituted with one or more groups selected from oxo, C1-6 alkyl, and (C1-3 alkoxy)Ci-3 alkyl;RSX1is selected from C(O)NR14R14’, a C3-8 carbocycle, and a 3-14 membered heterocycle containing one or more heteroatoms selected from N, O and S, wherein the carbocycle and heterocycle are each optionally substituted with one or more groups selected from oxo, halo, C1-3 alkyl, (C1-3 alkoxy)Ci-3 alkyl, C1-6 alkylamino, di-(Ci-6 alkyl) amino, and NH2; each R13is selected from the group consisting of OH, oxo, halo, C1-6 alkyl, C1-6 alkoxy, C2-6 alkenyl, C1-6 alkylamino, di-(Ci-6 alkyl) amino, NH2, C(0)NH2, CN, and NO2;R14and R14are each independently selected from the group consisting of H and C1-6 alkyl; m is selected from 1, 2, 3, 4, 5, 6, 7, 8, and 9;1 is selected from 1, 2, 3, 4, 5, 6, 7, 8, and 9; pi is selected from 1, 2, 3, 4, and 5; andP2 is selected from 1, 2, 3, 4, and 5.

[0531] In some embodiments, the ionizable lipid is a compound selected from Table IL-6.

[0532] In some aspects, the ionizable lipid is a compound of Formula (IL-III):ringt is 1 or 2;Ai and A2 are each independently selected from CH or N;Z is CH2 or absent wherein when Z is CH2, the dashed lines (1) and (2) each represent a single bond; and when Z is absent, the dashed lines (1) and (2) are both absent;Ri, R2, R3, R4, and R5 are independently selected from the group consisting of C5-20 alkyl, C5-20 alkenyl, -R”MR’, -R*YR”, -YR”, and -R*OR”;Rxi and Rx2 are each independently H or C1-3 alkyl; each M is independently selected from the group consisting of -C(O)O-, -OC(O)-, - OC(O)O-, -C(O)N(R’)-, -N(R’)C(O)-, -C(O)-, -C(S)-, -C(S)S-, -SC(S)-, -CH(OH)-, - P(O)(OR’)O-, -S(O)2-, -C(O)S-, -SC(O)-, an aryl group, and a heteroaryl group;M* is Ci-Ce alkyl,W1and W2are each independently selected from the group consisting of -O- and - N(Re)-; each Re is independently selected from the group consisting of H and C1-5 alkyl;X1, X2, and X3are independently selected from the group consisting of a bond, -CH2-, -(CH2)2-, -CHR-, -CHY-, -C(O)-, -C(O)O-, -OC(O)-, -(CH2)n-C(O)-, -C(O)-(CH2)n-, -(CH2)n- C(O)O-, -OC(O)-(CH2)n-, -(CH2)n-OC(O)-, -C(O)O-(CH2)n-, -CH(OH)-, -C(S)-, and - CH(SH)-; each Y is independently a C3-6 carbocycle; each R* is independently selected from the group consisting of C1-12 alkyl and C2-12 alkenyl; each R is independently selected from the group consisting of C1-3 alkyl and a C3-6 carbocycle; each R’ is independently selected from the group consisting of C1-12 alkyl, C2-12 alkenyl, and H; each R” is independently selected from the group consisting of C3-12 alkyl, C3-12 alkenyl and -R*MR’; and n is an integer from 1-6.

[0533] In some aspects, the ionizable lipid is a compound of Formula (IL-IIIA):or a salt or isomer thereof, whereinRi, R2, R3, R4, and R5 are independently selected from the group consisting of C5-20 alkyl, C5-20 alkenyl, -R”MR’, -R*YR”, -YR”, and -R*OR”; each M is independently selected from the group consisting of -C(O)O-, -OC(O)-, -OC(O)O-, -C(O)N(R’)-, -N(R’)C(O)-, -C(O)-, -C(S)-, -C(S)S-, -SC(S)-CH(OH)-, -P(O)(OR’)O-, -S(O)2-, an aryl group, and a heteroaryl group;X1, X2, and X3are independently selected from the group consisting of a bond, -CH2-,-(CH2)2-, -CHR-, -CHY-, -C(O)-, -C(O)O-, -OC(O)-, -C(O)-CH2-, -CH2-C(O)-, -C(O)O-CH2-, -OC(O)-CH2-, -CH2-C(O)O-, -CH2-OC(O)-, -CH(OH)-, -C(S)-, and -CH(SH)-; each Y is independently a C3-6 carbocycle; each R* is independently selected from the group consisting of C1-12 alkyl and C2-12 alkenyl; each R is independently selected from the group consisting of C1-3 alkyl and a C3-6 carbocycle; each R’ is independently selected from the group consisting of C1-12 alkyl, C2-12 alkenyl, and H; and each R” is independently selected from the group consisting of C3-12 alkyl and C3-12 alkenyl.

[0534] In some embodiments, the ionizable lipid is a compound selected from Table IL-7.Table IL-7: Ionizable lipids

[0535] In some embodiments, the ionizable lipid is a compound selected from:Ionizable Lipids

[0536] The present disclosure provides ionizable lipids. In some embodiments, the ionizable lipids include a central amine moiety and at least one biodegradable group. In some embodiments, the ionizable lipid is an amino lipid. The lipids described herein may be advantageously used in lipid nanoparticles and lipid nanoparticle formulations for the delivery of therapeutic and / or prophylactics, such as a nucleic acid, to mammalian cells or organs.

[0537] In some aspects, the ionizable lipids of the present disclosure may be one or more of compounds of Formula (IL-1):or their N-oxides, or salts or isomers thereof, wherein:R1is selected from the group consisting of C5-30 alkyl, C5-20 alkenyl, -R*YR”, -YR”, and -R”M’R’;R2and R3are independently selected from the group consisting of H, C1-14 alkyl, C2-14 alkenyl, -R*YR”, -YR”, and -R*OR”, or R2and R3, together with the atom to which they are attached, form a heterocycle or carbocycle;R4is selected from the group consisting of hydrogen, a C3-6 carbocycle, -(CH2)nQ, - (CH2)nCHQR, -(CH2)oC(R10)2(CH2)n-oQ, -CHQR, -CQ(R)2, and unsubstituted C1-6 alkyl, where Q is selected from a carbocycle, heterocycle, -OR, -O(CH2)nN(R)2, -C(O)OR, -OC(O)R, -CX3, -CX2H, -CXH2, -CN, -N(R)2, -C(O)N(R)2, -N(R)C(O)R, -N(R)S(O)2R, -N(R)C(O)N(R)2, - N(R)C(S)N(R)2, -N(R)R8, -N(R)S(O)2R8, -O(CH2)nOR, -N(R)C(=NR9)N(R)2, - N(R)C(=CHR9)N(R)2, -OC(O)N(R)2, -N(R)C(O)OR, -N(OR)C(O)R, -N(OR)S(O)2R, - N(OR)C(O)OR, -N(OR)C(O)N(R)2, -N(OR)C(S)N(R)2, -N(OR)C(=NR9)N(R)2, -N(OR)C(=CHR9)N(R)2, -C(=NR9)N(R)2, -C(=NR9)R, -C(O)N(R)OR, and - C(R)N(R)2C(O)OR, each o is independently selected from 1, 2, 3, and 4, and each n is independently selected from 1, 2, 3, 4, and 5; each R5is independently selected from the group consisting of OH, C1-3 alkyl, C2-3 alkenyl, and H; each R6is independently selected from the group consisting of OH, C1-3 alkyl, C2-3 alkenyl, and H;M and M’ are independently selected from -C(O)O-, -OC(O)-, -OC(O)-M”-C(O)O-, - C(O)N(R’)-,-N(R’)C(O)-, -C(O)-, -C(S)-, -C(S)S-, -SC(S)-, -CH(OH)-, -P(O)(OR’)O-, -S(O)2-, -S-S-, an aryl group, and a heteroaryl group, in which M” is a bond, C1-13 alkyl or C2-13 alkenyl;R7is selected from the group consisting of C1-3 alkyl, C2-3 alkenyl, and H;R8is selected from the group consisting of C3-6 carbocycle and heterocycle;R9is selected from the group consisting of H, CN, NO2, C1-6 alkyl, -OR, -S(O)2R, - S(O)2N(R)2, C2-6 alkenyl, C3-6 carbocycle and heterocycle;R10is selected from the group consisting of H, OH, C1-3 alkyl, and C2-3 alkenyl; each R is independently selected from the group consisting of C1-3 alkyl, C2-3 alkenyl, (CH2)qOR*, and H, and each q is independently selected from 1, 2, and 3; each R’ is independently selected from the group consisting of C1-18 alkyl, C2-18 alkenyl, -R*YR”, -YR”, and H; each R” is independently selected from the group consisting of C3-15 alkyl and C3-15 alkenyl; each R* is independently selected from the group consisting of C1-12 alkyl and C2-i2alkenyl; each Y is independently a C3-6 carbocycle; each X is independently selected from the group consisting of F, Cl, Br, and I; and m is selected from 5, 6, 7, 8, 9, 10, 11, 12, and 13; and wherein when R4is -(CH2)nQ, - (CH2)nCHQR, -CHQR, or -CQ(R)2, then (i) Q is not -N(R)2when n is 1, 2, 3, 4 or 5, or (ii) Q is not 5, 6, or 7-membered heterocycloalkyl when n is 1 or 2.

[0538] In some aspects, the ionizable lipids of the present disclosure may be one or more of compounds of Formula (IL-X):r its N-oxide, or a salt or isomer thereof, wherein or a salt or isomer thereof, whereinR1is selected from the group consisting of C5-30 alkyl, C5-20 alkenyl, -R*YR”, -YR”, and -R”M’R’;R2and R3are independently selected from the group consisting of H, C1-14 alkyl, C2-14 alkenyl, -R*YR”, -YR”, and -R*OR”, or R2and R3, together with the atom to which they are attached, form a heterocycle or carbocycle;R4is selected from the group consisting of hydrogen, a C3-6 carbocycle, -(CH2)nQ, - (CH2)nCHQR, -(CH2)oC(R10)2(CH2)n-oQ,-CHQR, -CQ(R)2, and unsubstituted C1-6 alkyl, where Q is selected from a carbocycle, heterocycle, -OR, -O(CH2)nN(R)2, -C(O)OR, -OC(O)R, -CX3, -CX2H, -CXH2, -CN, -N(R)2, - C(O)N(R)2, -N(R)C(O)R, -N(R)S(O)2R, -N(R)C(O)N(R)2, -N(R)C(S)N(R)2, N(R)R8, - N(R)S(O)2R8, -O(CH2)nOR, -N(R)C(=NR9)N(R)2, -N(R)C(=CHR9)N(R)2, -OC(O)N(R)2, - N(R)C(O)OR, -N(OR)C(O)R, -N(OR)S(O)2R, -N(OR)C(O)OR, -N(OR)C(O)N(R)2, - N(OR)C(S)N(R)2, -N(OR)C(=NR9)N(R)2, -N(OR)C(=CHR9)N(R)2, -C(=NR9)N(R)2, - C(=NR9)R, -C(O)N(R)OR, and -C(R)N(R)2C(0)0R, each o is independently selected from 1, 2, 3, and 4, and each n is independently selected from 1, 2, 3, 4, and 5;Rxis selected from the group consisting of C1-6 alkyl, C2-6 alkenyl, -(CH2)v0H, and - (CH2)VN(R)2, wherein v is selected from 1, 2, 3, 4, 5, and 6; each R5is independently selected from the group consisting of OH, C1-3 alkyl, C2-3 alkenyl, and H; each R6is independently selected from the group consisting of OH, C1-3 alkyl, C2-3 alkenyl, and H;M and M’ are independently selected from -C(O)O-, -OC(O)-, -OC(O)-M”-C(O)O-, - C(O)N(R’)-, -N(R’)C(O)-, -C(O)-, -C(S)-, -C(S)S-, -SC(S)-, -CH(OH)-, -P(O)(OR’)O-, - S(O)2-, -S-S-, an aryl group, and a heteroaryl group, in which M” is a bond, C1-13 alkyl or C2- 13 alkenyl;R7is selected from the group consisting of C1-3 alkyl, C2-3 alkenyl, and H;R8is selected from the group consisting of C3-6 carbocycle and heterocycle;R9is selected from the group consisting of H, CN, NO2, C1-6 alkyl, -OR, -S(O)2R, - S(O)2N(R)2, C2-6 alkenyl, C3-6 carbocycle and heterocycle;R10is selected from the group consisting of H, OH, C1-3 alkyl, and C2-3 alkenyl; each R is independently selected from the group consisting of C1-3 alkyl, C2-3 alkenyl, (CH2)qOR*, and H, and each q is independently selected from 1, 2, and 3; each R’ is independently selected from the group consisting of C1-18 alkyl, C2-18 alkenyl, -R*YR”, -YR”, and H; each R” is independently selected from the group consisting of C3-15 alkyl and C3-15 alkenyl; each R* is independently selected from the group consisting of C1-12 alkyl and C2-12 alkenyl; each Y is independently a C3-6 carbocycle; each X is independently selected from the group consisting of F, Cl, Br, and I; and m is selected from 5, 6, 7, 8, 9, 10, 11, 12, and 13.

[0539] In some embodiments, a subset of compounds of Formula (IL-I) includes those ofFormula (IL-IA):or its N-oxide, or a salt or isomer thereof, wherein 1 is selected from 1, 2, 3, 4, and 5; m is selected from 5, 6, 7, 8, and 9; Mi is a bond or M’; R4is hydrogen, unsubstituted C1-3 alkyl, - (CH2)oC(R10)2(CH2)n-oQ, or -(CH2)nQ, in which Q is OH, -NHC(S)N(R)2, -NHC(O)N(R)2, - N(R)C(O)R, -N(R)S(O)2R, -N(R)R8, -NHC(=NR9)N(R)2, -NHC(=CHR9)N(R)2, - OC(O)N(R)2, -N(R)C(O)OR, heteroaryl or heterocycloalkyl; M and M’ are independently selected from -C(O)O-, -OC(O)-, -OC(O)-M”-C(O)O-, -C(O)N(R’)-, -P(O)(OR’)O-, -S-S-, an aryl group, and a heteroaryl group,; and R2and R3are independently selected from the group consisting of H, C1-14 alkyl, and C2-14 alkenyl. For example, m is 5, 7, or 9. For example, Q is OH, -NHC(S)N(R)2, or -NHC(O)N(R)2. For example, Q is -N(R)C(O)R, or -N(R)S(O)2R.

[0540] In some embodiments, a subset of compounds of Formula (I) includes those of Formula (IL-IB):or its N-oxide, or a salt or isomer thereof, in which all variables are as defined herein. In some embodiments, m is selected from 5, 6, 7, 8, and 9; R4 is hydrogen, unsubstituted C1-3 alkyl, or -(CH2)nQ, in which Q is -OH, -NHC(S)N(R)2, -NHC(O)N(R)2, -N(R)C(O)R, -N(R)S(O)2R, - N(R)R8, -NHC(=NR9)N(R)2, -NHC(=CHR9)N(R)2, -OC(O)N(R)2, -N(R)C(O)OR, heteroaryl or heterocycloalkyl; M and M’ are independently selected from -C(O)O-, -OC(O)-, -OC(O)- M”- C(O)O-, -C(O)N(R’)-, -P(O)(OR’)O-, -S-S-, an aryl group, and a heteroaryl group,; and R2and R3 are independently selected from the group consisting of H, C1-14 alkyl, and C2-14 alkenyl. In some embodiments, m is 5, 7, or 9. In some embodiments, Q is OH, - NHC(S)N(R)2, or -NHC(O)N(R)2. In some embodiments, Q is -N(R)C(O)R, or -N(R)S(O)2R.

[0541] In some embodiments, a subset of compounds of Formula (IL-I) includes those of Formula (IL-II):or its N-oxide, or a slat or isomer thereof, wherein 1 is selected from 1, 2, 3, 4 and 5; Ml is a bond or M’; R4 is hydrogen, unsubstituted C1-3 alkyl, or -(CH2)nQ, in which n is 2, 3, or 4, and Q is -OH, - NHC(S)N(R)2, -NHC(O)N(R)2, -N(R)C(O)R, -N(R)S(O)2R, -N(R)R8, - NHC(=NR9)N(R)2, -NHC(=CHR9)N(R)2, -OC(O)N(R)2, -N(R)C(O)OR, heteroaryl or heterocycloalkyl; M and M’ are independently selected from -C(O)O-, -OC(O)-, -OC(O)-M”- C(O)O-, -C(O)N(R’)-, -P(O)(OR’)O-, -S-S-, an aryl group, and a heteroaryl group,; and R2and R3 are independently selected from the group consisting of H, C1-14 alkyl, and C2-14 alkenyl.

[0542] In some aspects, the ionizable lipids of the present disclosure may be one or more of compounds of Formula (IL-VI):r its N-oxide, or a salt or isomer thereof, whereinR1is selected from the group consisting of C5-30 alkyl, C5-20 alkenyl, -R*YR”, -YR”, and -R”M’R’;R2and R3are independently selected from the group consisting of H, C1-14 alkyl, C2-14 alkenyl, -R*YR”, -YR”, and -R*OR”, or R2and R3, together with the atom to which they are attached, form a heterocycle or carbocycle; each R5is independently selected from the group consisting of OH, C1-3 alkyl, C2-3 alkenyl, and H; each R6is independently selected from the group consisting of OH, C1-3 alkyl, C2-3 alkenyl, and H;M and M’ are independently selected from -C(O)O-, -OC(O)-, -OC(O)-M”-C(O)O-, -C(O)N(R’)-, -N(R’)C(O)-, -C(O)-, -C(S)-, -C(S)S-, -SC(S)-, -CH(OH)-, -P(O)(OR’)O-, -S(O )2-, -S-S-, an aryl group, and a heteroaryl group, in which M” is a bond, C1-13 alkyl or C2-13 alkenyl;R7is selected from the group consisting of C1-3 alkyl, C2-3 alkenyl, and H; each R is independently selected from the group consisting of H, C1-3 alkyl, and C2-3 alkenyl;RNis H, or C1-3 alkyl; each R’ is independently selected from the group consisting of C1-18 alkyl, C2-18 alkenyl, -R*YR”, -YR”, and H; each R” is independently selected from the group consisting of C3-15 alkyl and C3-15 alkenyl; each R* is independently selected from the group consisting of C1-12 alkyl and C2-12 alkenyl; each Y is independently a C3-6 carbocycle; each X is independently selected from the group consisting of F, Cl, Br, and I;Xaand Xbare each independently O or S;R10is selected from the group consisting of H, halo, -OH, R, -N(R)2, -CN, -N3, -C(O)OH, -C(O)OR, -OC(O)R, -OR, -SR, -S(O)R, -S(O)OR, -S(O)2OR, -NO2, -S(O)2N(R)2, -N(R)S(O)2R, -NH(CH2)tiN(R)2, -NH(CH2)piO(CH2)qiN(R)2,-NH(CH2)siOR, -N((CH2)siOR)2, a carbocycle, a heterocycle, aryl and heteroaryl; m is selected from 5, 6, 7, 8, 9, 10, 11, 12, and 13; n is selected from 1, 2, 3, 4, 5, 6, 7, 8, 9, and 10; r is 0 or 1; t1is selected from 1, 2, 3, 4, and 5; p1is selected from 1, 2, 3, 4, and 5; q1is selected from 1, 2, 3, 4, and 5; and s1is selected from 1, 2, 3, 4, and 5.

[0543] In some embodiments, a subset of compounds of Formula (IL-VI) includes those of Formula (IL-VI-a):or its N-oxide, or a salt or isomer thereof, whereinRlaand Rlbare independently selected from the group consisting of C1-14 alkyl and C2. 14 alkenyl; andR2and R3are independently selected from the group consisting of C1-14 alkyl, C2-14 alkenyl, -R*YR”, -YR”, and -R*OR”, or R2and R3, together with the atom to which they are attached, form a heterocycle or carbocycle.

[0544] In another embodiment, a subset of compounds of Formula (IL-VI) includes those of Formula (IL-VII):or its N-oxide, or a salt or isomer thereof, wherein1 is selected from 1, 2, 3, 4, and 5;Mi is a bond or M’; andR2and R3are independently selected from the group consisting of H, C1-14 alkyl, and C2-14 alkenyl.

[0545] In another embodiment, a subset of compounds of Formula (IL-VI) includes those of Formula (IL-VIII):or its N-oxide, or a salt or isomer thereof, wherein1 is selected from 1, 2, 3, 4, and 5;Mi is a bond or M’; andRaand Rbare independently selected from the group consisting of C1-14 alkyl and C2- 14 alkenyl; andR2and R3are independently selected from the group consisting of C1-14 alkyl, and C2- 14 alkenyl.

[0546] The compounds of any one of formula (IL-I), (IL-IA), (IL-VI), (IL-VI-a), (IL-VII) or (IL-VIII) include one or more of the following features when applicable.

[0547] In some embodiments, Mi is M’.

[0548] In some embodiments, M and M’ are independently -C(O)O- or -OC(O)-.

[0549] In some embodiments, at least one of M and M’ is -C(O)O- or -OC(O)-.

[0550] In certain embodiments, at least one of M and M’ is -OC(O)-.

[0551] In certain embodiments, M is -OC(O)- and M’ is -C(O)O-. In some embodiments, M is -C(O)O- and M’ is -OC(O)-. In certain embodiments, M and M’ are each -OC(O)-. In some embodiments, M and M’ are each -C(O)O-.

[0552] In certain embodiments, at least one of M and M’ is -OC(O)-M”-C(O)O-.

[0553] In some embodiments, M and M’ are independently -S-S-.

[0554] In some embodiments, at least one of M and M’ is -S-S-.

[0555] In some embodiments, one of M and M’ is -C(O)O- or -OC(O)- and the other is -S-S-. For example, M is -C(O)O- or -OC(O)- and M’ is -S-S- or M’ is -C(O)O-, or -OC(O)- and M is -S-S-.

[0556] In some embodiments, one of M and M’ is -OC(O)-M”-C(O)O-, in which M” is a bond, Ci-13 alkyl or C2-13 alkenyl. In other embodiments, M” is C1-6 alkyl or C2-6 alkenyl. In certainembodiments, M” is C1-4 alkyl or C2-4 alkenyl. For example, in some embodiments, M” is Ci alkyl. For example, in some embodiments, M” is C2 alkyl. For example, in some embodiments, M” is C3 alkyl. For example, in some embodiments, M” is C4 alkyl. For example, in some embodiments, M” is C2 alkenyl. For example, in some embodiments, M” is C3 alkenyl. For example, in some embodiments, M” is C4 alkenyl.

[0557] In some embodiments, 1 is 1, 3, or 5.

[0558] In some embodiments, R4is hydrogen.

[0559] In some embodiments, R4is not hydrogen.

[0560] In some embodiments, R4is unsubstituted methyl or -(CH2)nQ, in which Q is OH, -NHC(S)N(R)2, -NHC(O)N(R)2, -N(R)C(O)R, or -N(R)S(O)2R.

[0561] In some embodiments, Q is OH.

[0562] In some embodiments, Q is -NHC(S)N(R)2.

[0563] In some embodiments, Q is -NHC(O)N(R)2.

[0564] In some embodiments, Q is -N(R)C(O)R.

[0565] In some embodiments, Q is -N(R)S(O)2R.

[0566] In some embodiments, Q is -O(CH2)nN(R)2.

[0567] In some embodiments, Q is -O(CH2)nOR.

[0568] In some embodiments, Q is -N(R)R8.

[0569] In some embodiments, Q is -NHC(=NR9)N(R)2.

[0570] In some embodiments, Q is -NHC(=CHR9)N(R)2.

[0571] In some embodiments, Q is -OC(O)N(R)2.

[0572] In some embodiments, Q is -N(R)C(O)OR.

[0573] In some embodiments, n is 2.

[0574] In some embodiments, n is 3.

[0575] In some embodiments, n is 4.

[0576] In some embodiments, Mi is absent.

[0577] In some embodiments, at least one R5is hydroxyl. For example, one R5is hydroxyl.

[0578] In some embodiments, at least one R6is hydroxyl. For example, one R6is hydroxyl.

[0579] In some embodiments one of R5and R6is hydroxyl. For example, one R5is hydroxyl and each R6is hydrogen. For example, one R6is hydroxyl and each R5is hydrogen.

[0580] In some embodiments, Rxis C1-6 alkyl. In some embodiments, Rxis C1-3 alkyl. For example, Rxis methyl. For example, Rxis ethyl. For example, Rxis propyl.

[0581] In some embodiments, Rxis -(CH2)VOH and, v is 1, 2 or 3. For example, Rxis methanoyl. For example, Rxis ethanoyl. For example, Rxis propanoyl.

[0582] In some embodiments, Rxis -(CH2)VN(R)2, v is 1, 2 or 3 and each R is H or methyl. For example, Rxis methanamino, methylmethanamino, or dimethylmethanamino. For example, Rxis aminomethanyl, methylaminomethanyl, or dimethylaminomethanyl. For example, Rxis aminoethanyl, methylaminoethanyl, or dimethylaminoethanyl. For example, Rxis aminopropanyl, methylaminopropanyl, or dimethylaminopropanyl.

[0583] In some embodiments, R’ is Cuis alkyl, C2-18 alkenyl, -R*YR”, or -YR”.

[0584] In some embodiments, R2and R3are independently C3-14 alkyl or C3-14 alkenyl.

[0585] In some embodiments, Rlbis C1-14 alkyl. In some embodiments, Rlbis C2-14 alkyl. In some embodiments, Rlbis C3-14 alkyl. In some embodiments, Rlbis C1-8 alkyl. In some embodiments, Rlbis C1-5 alkyl. In some embodiments, Rlbis C1-3 alkyl. In some embodiments, Rlbis selected from Ci alkyl, C2 alkyl, C3 alkyl, C4 alkyl, and C5 alkyl. For example, in some embodiments, Rlbis Ci alkyl. For example, in some embodiments, Rlbis C2 alkyl. For example, in some embodiments, Rlbis C3 alkyl. For example, in some embodiments, Rlbis C4 alkyl. For example, in some embodiments, Rlbis C5 alkyl.

[0586] In some embodiments, R1is different from -(CHR5R6)m-M-CR2R3R7.

[0587] In some embodiments, -CHRlaRlb- is different from -(CHR5R6)m-M-CR2R3R7.

[0588] In some embodiments, R7is H. In some embodiments, R7is selected from C1-3 alkyl. For example, in some embodiments, R7is Ci alkyl. For example, in some embodiments, R7is C2 alkyl. For example, in some embodiments, R7is C3 alkyl. In some embodiments, R7is selected from C4 alkyl, C4 alkenyl, C5 alkyl, C5 alkenyl, Ce alkyl, Ce alkenyl, C7 alkyl, C7 alkenyl, C9 alkyl, C9 alkenyl, Cn alkyl, Cn alkenyl, C17 alkyl, C17 alkenyl, Cis alkyl, and Cis alkenyl.

[0589] In some embodiments, Rb’ is Cl-14 alkyl. In some embodiments, Rb’ is C2-14 alkyl. In some embodiments, Rbis C3-14 alkyl. In some embodiments, Rbis C1-8 alkyl. In some embodiments, Rbis C1-5 alkyl. In some embodiments, Rbis C1-3 alkyl. In some embodiments, Rbis selected from Ci alkyl, C2 alkyl, C3 alkyl, C4 alkyl and C5 alkyl. For example, in some embodiments, Rbis Ci alkyl. For example, in some embodiments, Rbis C2 alkyl. For example, some embodiments, Rbis C3 alkyl. For example, some embodiments, Rbis C4 alkyl.

[0590] In one embodiment, the compounds of Formula (IL-I) are of Formula (IL-IIa):or their N-oxides, or salts or isomers thereof, wherein R4 is as described herein.

[0591] In another embodiment, the compounds of Formula (IL-I) are of Formula (IL-IIb):or their N-oxides, or salts or isomers thereof, wherein R4 is as described herein.

[0592] In another embodiment, the compounds of Formula (IL-I) are of Formula (IL-IIc) or (IL-IIe):or their N-oxides, or salts or isomers thereof, wherein R4 is as described herein.

[0593] In another embodiment, the compounds of Formula (IL-I) are of Formula (IL-IIf):or their N-oxides, or salts or isomers thereof, wherein M is -C(O)O- or -OC(O)-, M” is C1-6 alkyl or C2-6 alkenyl, R2 and R3 are independently selected from the group consisting of C5-14 alkyl and C5-14 alkenyl, and n is selected from 2, 3, and 4.

[0594] In a further embodiment, the compounds of Formula (IL-I) are of Formula (IL-IId):or their N-oxides, or salts or isomers thereof, wherein n is 2, 3, or 4; and m, R’, R”, and R2 through Re are as described herein. In some embodiments, each of R2 and R3 may be independently selected from the group consisting of C5-14 alky and C5-14 alkenyl.

[0595] In a further embodiment, the compounds of Formula (IL-I) are of Formula (IL-IIg):or their N-oxides, or salts or isomers thereof, wherein 1 is selected from 1, 2, 3, 4, and 5; m is selected from 5, 6, 7, 8, and 9; Mi is a bond or M’; M and M’ are independently selected from from -C(O)O-, -OC(O)-, -OC(O)-M”-C(O)O-, -C(O)N(R’)-, -P(O)(OR’)O-, -S-S-, an aryl group, and a heteroaryl group; and R2 and R3 are independently selected from the group consisting of H, C1-14 alkyl, and C2-14 alkenyl. In some embodiments, M” is C1-6 alkyl (e.g., C1-4 alkyl) or C2-6 alkenyl (e.g. C2-4 alkenyl). In some embodiments, R2 and R3 are independently selected from the group consisting of C5-14 alkyl and C5-14 alkenyl.

[0596] In another embodiment, a subset of compounds of Formula (IL-VI) includes those of Formula (IL-VIIa):its N-oxide, or a salt or isomer thereof.

[0597] In another embodiment, a subset of compounds of Formula (VI) includes those of Formula (IL-VIIIa):its N-oxide, or a salt or isomer thereof.

[0598] In another embodiment, a subset of compounds of Formula (IL-VI) includes those of Formula (IL-VIIIb):salt or isomer thereof.

[0599] In another embodiment, a subset of compounds of Formula (IL-VI) includes those ofa salt or isomer thereof.

[0600] In another embodiment, a subset of compounds of Formula (IL-VI) includes those ofFormula (IL-VIIb-2):its N-oxide, or a salt or isomer thereof.

[0601] In another embodiment, a subset of compounds of Formula (IL-VI) includes those of Formula (IL-VIIb-3):its N-oxide, or a salt or isomer thereof.

[0602] In another embodiment, a subset of compounds of Formula (IL-VI) includes those ofFormula (IL-VIIc):

[0603] In another embodiment, a subset of compounds of Formula (IL-VI) includes those ofsalt or isomer thereof.

[0604] In another embodiment, a subset of compounds of Formula (IL-VI) includes those ofFormula (IL-VIIIc):

[0605] In another embodiment, a subset of compounds of Formula (IL-VI) includes those ofFormula (IL-VIIId):r its N-oxide, or a salt or isomer thereof.

[0606] The compounds of any one of formulae (IL-I), (IL-IA), (IL-IB), (IL-II), (IL-IIa), (IL- Ilb), (IL-IIc), (IL-IId), (IL-IIe), (IL-IIf), (IL-IIg), (IL-III), (IL-VI), (IL-VI-a), (IL-VII), (IL- VIII), (IL-VIIa), (IL-VIIIa), (IL-VIIIb), (IL-VIIb-1), (IL-VIIb-2), (IL-VIIb-3), (IL-VIIc), (IL- Vlld), (IL-VIIIc), or (IL-VIIId) include one or more of the following features when applicable.

[0607] In some embodiments, the ionizable lipids are one or more of the compounds described in PCT Application Nos. PCT / US2020 / 051613, PCT / US2020 / 051613, andPCT / US2020 / 051629, and in PCT Publication Nos. WO 2017 / 049245, WO 2018 / 170306, WO 2018 / 170336, WO 2020 / 061367.

[0608] In some embodiments, the ionizable lipids are selected from Compounds 1-280 described in U.S. Application No. 62 / 475,166.

[0609] In some embodiments, the ionizable lipid issalt thereof.

[0610] In some embodiments, the ionizable lipid is (IL-1).

[0611] In some embodiments, the ionizable lipid issalt thereof.

[0612] In some embodiments, the ionizable lipid is IL-2.

[0613] In some embodiments, the ionizable lipid issalt thereof.

[0614] In some embodiments, the ionizable lipid is IL-3.

[0615] In some embodiments, the ionizable lipid issalt thereof.

[0616] In some embodiments, the ionizable lipid is IL-4.

[0617] In some embodiments, the ionizable lipid is

[0619] In some embodiments, the ionizable lipid isor a salt thereof.

[0620] In some embodiments, the ionizable lipid is IL-6.

[0621] In some embodiments, the ionizable lipid isor a salt thereof.

[0622] In some embodiments, the ionizable lipid is IL-7.

[0623] In some embodiments, the ionizable lipid isor a salt thereof.

[0624] In some embodiments, the ionizable lipid is IL-8.

[0625] In some embodiments, the ionizable lipid isor a salt thereof.

[0626] In some embodiments, the ionizable lipid is IL-9.

[0627] In some embodiments, the ionizable lipid isor a salt thereof.

[0628] In some embodiments, the ionizable lipid is IL-10.

[0629] In some embodiments, the ionizable lipid isor a salt thereof.

[0630] In some embodiments, the ionizable lipid is IL-11.

[0631] In some embodiments, the ionizable lipid isor a salt thereof.

[0632] In some embodiments, the ionizable lipid is IL-12.

[0633] In some embodiments, the ionizable lipid is

[0634] In some embodiments, the ionizable lipid is IL-13.

[0635] In some embodiments, the ionizable lipid isor a salt thereof.

[0636] In some embodiments, the ionizable lipid is IL-14.

[0637] In some embodiments, the ionizable lipid isor a salt thereof.

[0638] In some embodiments, the ionizable lipid is IL-15.

[0639] In some embodiments, the ionizable lipid isor a salt thereof.

[0640] In some embodiments, the ionizable lipid is IL-16.

[0641] In some embodiments, the ionizable lipid isor a salt thereof.

[0642] In some embodiments, the ionizable lipid is IL-17.

[0643] In some embodiments, the ionizable lipid is

[0644] In some embodiments, the ionizable lipid is IL-18.

[0645] In some embodiments, the ionizable lipid isor a salt thereof.

[0646] In some embodiments, the ionizable lipid is IL- 19.

[0647] In some aspects, the ionizable lipids of the present disclosure may be one or more of compounds of formula (IL-VIVa):or its N-oxide, or a salt or isomer thereof, wherein R’ais R’branchedOr R’cvcllc; whereinwherein ? denotes a point of attachment; wherein Rayand Rbyare each independently a C2-12 alkyl or C2-12 alkenyl;R2and R3are each independently selected from the group consisting of C1-14 alkyl andC2-14 alkenyl;R4is -(CH2)2OH; each R’ independently is a C1-12 alkyl or C2-12 alkenyl;Yais a C3-6 carbocycle;R*”ais selected from the group consisting of C1-15 alkyl and C2-15 alkenyl; and s is 2 or 3.

[0648] In some aspects, the ionizable lipids of the present disclosure may be one or more of compounds of formula (IL-VIVb):or its N-oxide, or a salt or isomer thereof,wherein ? denotes a point of attachment; wherein Rayand Rbyare each independently a C2-12 alkyl or C2-12 alkenyl;R2and R3are each independently selected from the group consisting of C1-14 alkyl andC2-14 alkenyl;denotes a point of attachment;R10is N(R)?; each R is independently selected from the group consisting of C1-6 alkyl,C2-3 alkenyl, and H; and n2 is selected from the group consisting of 1, 2, 3, 4, 5, 6, 7, 8, 9, and10; each R’ independently is a C1-12 alkyl or C2-12 alkenyl;Yais a C3-6 carbocycle;R*”ais selected from the group consisting of C1-15 alkyl and C2-15 alkenyl; and s is 2 or 3.

[0649] In some embodiments, the ionizable lipid is selected from:

[0650] In some aspects, the ionizable lipids of the present disclosure may be one or more of compounds of formula (IL-III):or salts or isomers thereof, wherein,t is 1 or 2;Ai and A2 are each independently selected from CH or N;Z is CH2 or absent wherein when Z is CH2, the dashed lines (1) and (2) each represent a single bond; and when Z is absent, the dashed lines (1) and (2) are both absent;Ri, R2, R3, R4, and R5 are independently selected from the group consisting of C5-20 alkyl, C5-20 alkenyl, -R”MR’, -R*YR”, -YR”, and -R*OR”;Rxi and Rx2 are each independently H or C1-3 alkyl; each M is independently selected from the group consisting of -C(O)O-, -OC(O)-, - OC(O)O-, -C(O)N(R’)-, -N(R’)C(O)-, -C(O)-, -C(S)-, -C(S)S-, -SC(S)-, -CH(OH)-, - P(O)(OR’)O-, -S(O)2-, -C(O)S-, -SC(O)-, an aryl group, and a heteroaryl group;M* is Ci-Ce alkyl,W1and W2are each independently selected from the group consisting of -O- and -N(Re)-; each Re is independently selected from the group consisting of H and C1-5 alkyl;X1, X2, and X3are independently selected from the group consisting of a bond, -CH2-, -(CH2)2-, -CHR-, -CHY-, -C(O)-, -C(O)O-, -OC(O)-, -(CH2)n-C(O)-, -C(O)-(CH2)n-, -(CH2)n- C(O)O-, -OC(O)-(CH2)n-, -(CH2)n-OC(O)-, -C(O)O-(CH2)n-, -CH(OH)-, -C(S)-, and -CH(SH)- each Y is independently a C3-6 carbocycle; each R* is independently selected from the group consisting of C1-12 alkyl and C2-12 alkenyl; each R is independently selected from the group consisting of C1-3 alkyl and a C3-6 carbocycle; each R’ is independently selected from the group consisting of C1-12 alkyl, C2-12 alkenyl, and H; each R” is independently selected from the group consisting of C3-12 alkyl, C3-12 alkenyl and -R*MR’ ; and n is an integer from 1-6; wherein when ring, then i) at least one of X1, X2, and X3is not -CH2-; and / or ii) at least one of Ri, R2, R3, R4, and R5 is -R”MR’.

[0651] In some embodiments, the compound is of any of formulae (IL-IIIal)-(IL-IIIa8):

[0652] In some embodiments, the ionizable lipids are one or more of the compounds described in PCT Publication Nos. WO 2017 / 112865, WO 2018 / 232120.

[0653] In some embodiments, the ionizable lipids are selected from Compound 1-156 described in PCT Publication No. WO 2018 / 232120.

[0654] In some embodiments, the ionizable lipids are selected from Compounds 1-16, 42-66, 68-76, and 78-156 described in PCT Publication Nos. WO 2017 / 112865.

[0655] In some embodiments, the ionizable lipid is

[0656] In some embodiments, the ionizable lipid is IL-20.

[0657] In some embodiments, the ionizable lipid issalt thereof.

[0658] In some embodiments, the ionizable lipid is IL-21.

[0659] The central amine moiety of a lipid according to Formula (IL-1), (IL-IA), (IL-IB), (IL- II), (IL-IIa), (IL-IIb), (IL-IIc), (IL-IId), (IL-IIe), (IL-IIf), (IL-IIg), (IL-HI), (IL-IIIal), (IL- IIIa2), (IL-IIIa3), (IL-IIIa4), (IL-IIIa5), (IL-IIIa6), (IL-IIIa7), or (IL-IIIa8) may be protonated at a physiological pH. Thus, a lipid may have a positive or partial positive charge at physiological pH. Such lipids may be referred to as cationic or ionizable (amino)lipids. Lipids may also be zwitterionic, i.e., neutral molecules having both a positive and a negative charge.

[0660] In some embodiments, the ionizable lipid is selected from the group consisting of 3- (didodecylamino)-N 1 ,N1 ,4-tridodecyl- 1 -piperazineethanamine (KL 10), Nl-[2-(didodecylamino)ethyl]-Nl,N4,N4-tridodecyl-l,4-piperazinedi ethanamine (KL22), 14,25- ditridecyl- 15,18,21 ,24-tetraaza-octatriacontane (KL25), 1 ,2-dilinoleyloxy-N,N- dimethylaminopropane (DLin-DMA), 2, 2-dilinoleyl-4-dimethylaminomethyl-[l,3]-di oxolane (DLin-K-DMA), heptatriaconta-6,9,28,31-tetraen-19-yl 4-(dimethylamino)butanoate (DLin- MC3-DMA), 2, 2-dilinoleyl-4-(2-dimethylaminoethyl)-[l,3]-di oxolane (DLin-KC2-DMA), l,2-dioleyloxy-N,N-dimethylaminopropane (DODMA), 2-({8-[(3P)-cholest-5-en-3- yloxy]octyl}oxy)-N,N-dimethyl-3-[(9Z,12Z)-octadeca-9,12-dien-l-yloxy]propan-l-amine (Octyl -CLinDMA), (2R)-2-({8-[(3P)-cholest-5-en-3-yloxy]octyl}oxy)-N,N-dimethyl-3- [(9Z,12Z)-octadeca-9,12-dien-l-yloxy]propan-l -amine (Octyl-CLinDMA (2R)), and (2S)-2- ({8-[(3P)-cholest-5-en-3-yloxy]octyl}oxy)-N,N-dimethyl-3-[(9Z,12Z)-octadeca-9,12-dien-l- yloxy]propan-l -amine (Octyl-CLinDMA (2S)).Polyethylene Glycol (PEG) Lipids

[0661] As used herein, the term “PEG lipid” refers to polyethylene glycol (PEG)-modified lipids. Non-limiting examples of PEG lipids include PEG-modified phosphatidylethanolamine and phosphatidic acid, PEG-ceramide conjugates (e.g., PEG-CerC14 or PEG-CerC20), PEG- modified dialkylamines and PEG-modified l,2-diacyloxypropan-3 -amines. Such lipids are also referred to as PEGylated lipids. In some embodiments, a PEG lipid can be PEG-c-DOMG, PEG-DMG, PEG-DLPE, PEG-DMPE, PEG-DPPC, or a PEG-DSPE lipid.

[0662] In some embodiments, the PEG lipid includes, but are not limited to, 1,2-dimyristoyl- sn-glycerol methoxypolyethylene glycol (PEG-DMG), 1,2-di stearoyl -sn-glycero-3- phosphoethanolamine-N-[amino(polyethylene glycol)] (PEG-DSPE), PEG-disteryl glycerol (PEG-DSG), PEG-dipalmetoleyl, PEG-dioleyl, PEG-distearyl, PEG-diacylglycamide (PEGDAG), PEG-dipalmitoyl phosphatidylethanolamine (PEG-DPPE), or PEG-1, 2- dimyristyloxlpropyl-3-amine (PEG-c-DMA).

[0663] In one embodiment, the PEG lipid is selected from the group consisting of a PEG- modified phosphatidylethanolamine, a PEG-modified phosphatidic acid, a PEG-modified ceramide, a PEG-modified dialkylamine, a PEG-modified diacylglycerol, a PEG-modified dialkylglycerol, and mixtures thereof.

[0664] In some embodiments, the lipid moiety of the PEG lipids includes those having lengths of from about Ci4 to about C22, In some embodiments, the lipid moiety of the PEG lipids includes those having lengths of from about Cw to about Ci6. In some embodiments, a PEG moiety, for example an mPEG-NEE, has a size of about 1000, 2000, 5000, 10,000, 15,000 or 20,000 daltons. In one embodiment, the PEG lipid is PEG2k-DMG.

[0665] In one embodiment, the lipid nanoparticles described herein can comprise a PEG lipid which is a non-diffusible PEG. Non-limiting examples of non-diffusible PEGs include PEG- DSG and PEG-DSPE.

[0666] PEG lipids are known in the art, such as those described in U.S. Patent No. 8158601 and International Publ. No. WO 2015 / 130584 A2, which are incorporated herein by reference in their entirety.

[0667] In general, some of the other lipid components (e.g., PEG lipids) of various formulae, described herein may be synthesized as described International Patent Application No. PCT / US2016 / 000129, filed December 10, 2016, entitled “Compositions and Methods for Delivery of Therapeutic Agents,” which is incorporated by reference in its entirety.

[0668] The lipid component of a lipid nanoparticle or lipid nanoparticle formulation may include one or more molecules comprising polyethylene glycol, such as PEG or PEG-modified lipids. Such species may be alternately referred to as PEGylated lipids. A PEG lipid is a lipid modified with polyethylene glycol. A PEG lipid may be selected from the non-limiting group including PEG-modified phosphatidylethanolamines, PEG-modified phosphatidic acids, PEG- modified ceramides, PEG-modified dialkylamines, PEG-modified di acylglycerols, PEG- modified dialkylglycerols, and mixtures thereof. In some embodiments, a PEG lipid may be PEG-c-DOMG, PEG-DMG, PEG-DLPE, PEG-DMPE, PEG-DPPC, or a PEG-DSPE lipid.

[0669] In some embodiments, the PEG-modified lipids are a modified form of PEG DMG. PEG-DMG has the following structure:

[0670] In one embodiment, PEG lipids useful in the present invention can be PEGylated lipids described in International Publication No. WO2012099755, the contents of which is herein incorporated by reference in its entirety. Any of these exemplary PEG lipids described herein may be modified to comprise a hydroxyl group on the PEG chain. In some embodiments, the PEG lipid is a PEG-OH lipid. As generally defined herein, a “PEG-OH lipid” (also referred to herein as “hydroxy -PEGylated lipid”) is a PEGylated lipid having one or more hydroxyl (-OH) groups on the lipid. In some embodiments, the PEG-OH lipid includes one or more hydroxyl groups on the PEG chain. In some embodiments, a PEG-OH or hydroxy-PEGylated lipid comprises an -OH group at the terminus of the PEG chain. Each possibility represents a separate embodiment of the present invention.

[0671] In some embodiments, a PEG lipid useful in the present invention is a compound of Formula (PL-I). Provided herein are compounds of Formula (PL-I):or salts thereof, wherein:R3is -OR°;R° is hydrogen, optionally substituted alkyl, or an oxygen protecting group; r is an integer between 1 and 100, inclusive;L1is optionally substituted Ci-io alkylene, wherein at least one methylene of the optionally substituted Ci-io alkylene is independently replaced with optionally substituted carbocyclylene, optionally substituted heterocyclylene, optionally substituted arylene, optionally substituted heteroarylene, O, N(RN), S, C(O), C(O)N(RN), NRNC(O), C(O)O, - OC(O), OC(O)O, OC(O)N(RN), NRNC(O)O, or NRNC(O)N(RN);D is a moiety obtained by click chemistry or a moiety cleavable under physiological conditions; m is 0, 1, 2, 3, 4, 5, 6, 7, 8, 9, or 10;A is of the formula:each instance of of L2is independently a bond or optionally substituted Ci-6 alkylene, wherein one methylene unit of the optionally substituted Ci-6 alkylene is optionally replaced with O, N(RN), S, C(O), C(O)N(RN), NRNC(O), C(O)O, OC(O), OC(O)O, OC(O)N(RN), - NRNC(O)O, or NRNC(O)N(RN); each instance of R2is independently optionally substituted C1-30 alkyl, optionally substituted C1-30 alkenyl, or optionally substituted C1-30 alkynyl; optionally wherein one or more methylene units of R2are independently replaced with optionally substituted carbocyclylene, optionally substituted heterocyclylene, optionally substituted arylene, optionally substituted heteroarylene, N(RN), O, S, C(O), C(O)N(RN), NRNC(O), - NRNC(O)N(RN), C(O)O, OC(O), OC(O)O, OC(O)N(RN), NRNC(O)O, C(O)S, SC(O), - C(=NRN), C(=NRN)N(RN), NRNC(=NRN), NRNC(=NRN)N(RN), C(S), C(S)N(RN), NRNC(S), NRNC(S)N(RN), S(O) , OS(O), S(O)O, OS(O)O, OS(O)2, S(O)2O, OS(O)2O, N(RN)S(O), - S(O)N(RN), N(RN)S(O)N(RN), OS(O)N(RN), N(RN)S(O)O, S(O)2, N(RN)S(O)2, S(O)2N(RN), N(RN)S(O)2N(RN), OS(O)2N(RN), or N(RN)S(O)2O; each instance of RNis independently hydrogen, optionally substituted alkyl, or a nitrogen protecting group;Ring B is optionally substituted carbocyclyl, optionally substituted heterocyclyl, optionally substituted aryl, or optionally substituted heteroaryl; and p is 1 or 2.

[0672] In some embodiments, the compound of Formula (PL-I) is a PEG-OH lipid (z.e., R3is -OR°, and R° is hydrogen). In some embodiments, the compound of Formula (PL-I) is of Formula (PL-I-OH):or a salt thereof.

[0673] In some embodiments, a PEG lipid useful in the present invention is a PEGylated fatty acid. In some embodiments, a PEG lipid useful in the present invention is a compound of Formula (PL-II). Provided herein are compounds of Formula (PL-II):or a salt thereof, wherein:R3is-OR°;R° is hydrogen, optionally substituted alkyl or an oxygen protecting group;r is an integer between 1 and 100, inclusive;R5is optionally substituted C10-40 alkyl, optionally substituted C10-40 alkenyl, or optionally substituted C10-40 alkynyl; and optionally one or more methylene groups of R5are replaced with optionally substituted carbocyclylene, optionally substituted heterocyclylene, optionally substituted arylene, optionally substituted heteroarylene, N(RN), O, S, C(O), - C(O)N(RN), NRNC(O), NRNC(O)N(RN), C(O)O, OC(O), OC(O)O, OC(O)N(RN), NRNC(O)O, C(O)S, SC(O), C(=NRN), C(=NRN)N(RN), NRNC(=NRN), NRNC(=NRN)N(RN), C(S), - C(S)N(RN), NRNC(S), NRNC(S)N(RN), S(O), OS(O), S(O)O, OS(O)O, OS(O)2, S(O)2O, - OS(O)2O, N(RN)S(O), S(O)N(RN), N(RN)S(O)N(RN), OS(O)N(RN), N(RN)S(O)O, S(O)2, - N(RN)S(O)2, S(O)2N(RN), N(RN)S(O)2N(RN), OS(O)2N(RN), orN(RN)S(O)2O; and each instance of RNis independently hydrogen, optionally substituted alkyl, or a nitrogen protecting group.

[0674] In some embodiments, the compound of Formula (PL-II) is of Formula (PL-II-OH):or a salt thereof, wherein: r is an integer between 1 and 100;R5is optionally substituted C10-40 alkyl, optionally substituted C10-40 alkenyl, or optionally substituted C10-40 alkynyl; and optionally one or more methylene groups of R5are replaced with optionally substituted carbocyclylene, optionally substituted heterocyclylene, optionally substituted arylene, optionally substituted heteroarylene, N(RN), O, S, C(O), - C(O)N(RN), NRNC(O), NRNC(O)N(RN), C(O)O, OC(O), OC(O)O, OC(O)N(RN), NRNC(O)O, C(O)S, SC(O), C(=NRN), C(=NRN)N(RN), NRNC(=NRN), NRNC(=NRN)N(RN), C(S), - C(S)N(RN), NRNC(S), NRNC(S)N(RN), S(O), OS(O), S(O)O, OS(O)O, OS(O)2, S(O)2O, - OS(O)2O, N(RN)S(O), S(O)N(RN), N(RN)S(O)N(RN), OS(O)N(RN), N(RN)S(O)O, S(O)2, - N(RN)S(O)2, S(O)2N(RN), N(RN)S(O)2N(RN), OS(O)2N(RN), orN(RN)S(O)2O; and each instance of RNis independently hydrogen, optionally substituted alkyl, or a nitrogen protecting group.

[0675] In some embodiments, r is an integer between 10 to 80, between 20 to 70, between 30 to 60, or between 40 to 50.

[0676] In some embodiments, r is 45.

[0677] In some embodiments, R5is C17 alkyl.

[0678] In yet other embodiments the compound of Formula (PL-II) is:or a salt thereof.

[0679] In one embodiment, the compound of Formula (PL-II) is

[0680] In some aspects, the lipid composition of the pharmaceutical compositions described herein does not comprise a PEG lipid.

[0681] In some embodiments, the PEG lipids may be one or more of the PEG lipids described in U.S. Application No. 62 / 520,530.

[0682] In some embodiments, the PEG lipid is a compound of Formula (PL-III):or a salt or isomer thereof, wherein s is an integer between 1 and 100.

[0683] In some embodiments, the PEG lipid is a compound of the following formula:or a salt or isomer thereof.Structural Lipids

[0684] As used herein, the term “structural lipid” refers to sterols and also to lipids containing sterol moieties.

[0685] Incorporation of structural lipids in the lipid nanoparticle may help mitigate aggregation of other lipids in the particle. Structural lipids can be selected from the group including but not limited to, cholesterol, fecosterol, sitosterol, ergosterol, campesterol, stigmasterol, brassicasterol, tomatidine, tomatine, ursolic acid, alpha-tocopherol, hopanoids, phytosterols, steroids, and mixtures thereof. In some embodiments, the structural lipid is a mixture of two or more components each independently selected from cholesterol, fecosterol, sitosterol,ergosterol, campesterol, stigmasterol, brassicasterol, tomatidine, tomatine, ursolic acid, alphatocopherol, hopanoids, phytosterols, and steroids. In some embodiments, the structural lipid is a sterol. In some embodiments, the structural lipid is a mixture of two or more sterols. As defined herein, “sterols” are a subgroup of steroids consisting of steroid alcohols. In some embodiments, the structural lipid is a steroid. In some embodiments, the structural lipid is cholesterol. In some embodiments, the structural lipid is an analog of cholesterol. In some embodiments, the structural lipid is alpha-tocopherol.

[0686] In some embodiments, the structural lipids may be one or more structural lipids described in U.S. Application No. 62 / 520,530.

[0687] As defined herein, “sterols” are a subgroup of steroids consisting of steroid alcohols. In some embodiments, the structural lipid is a steroid. In some embodiments, the structural lipid is cholesterol. In some embodiments, the structural lipid is an analog of cholesterol. In some embodiments, the structural lipid is alpha-tocopherol.

[0688] In some embodiments, the structural lipid isor a salt thereof.

[0689] In some embodiments, the structural lipid is SL-1.

[0690] In some embodiments, the structural lipid isor a salt thereof.

[0691] In some embodiments, the structural lipid (e.g., SL-2) is present at a concentration ranging from about 15 mol% to about 70 mol %, from about 20 mol% to about 60 mol %, fromabout 25 mol% to about 50 mol %, from about 30 mol% to about 45 mol %, from about 35 mol% to about 40 mol %, or from about 36 mol% to about 38 mol %.

[0692] In some embodiments, the structural lipid (e.g., SL-2) is present at a concentration of about 36.6±25 mol %, about 36.6±20 mol %, about 36.6±15 mol %, about 36.6±10 mol %, about 36.6±9 mol %, about 36.6±8 mol %, about 36.6±7 mol %, about 36.6±6 mol %, about 36.6±5 mol %, about 36.6±4 mol %, about 36.6±3 mol %, about 36.6±2 mol %, about 36.6±1 mol %, about 36.6±0.8 mol %, about 36.6±0.6 mol %, about 36.6±0.5 mol %, about 36.6±0.4 mol %, about 36.6±0.3 mol %, about 36.6±.2 mol %, or about 36.6±0.1 mol % (e.g., about 36.6 mol %).Phospholipids

[0693] Phospholipids may assemble into one or more lipid bilayers. In general, phospholipids comprise a phospholipid moiety and one or more fatty acid moieties.

[0694] A phospholipid moiety can be selected, for example, from the non-limiting group consisting of phosphatidyl choline, phosphatidyl ethanolamine, phosphatidyl glycerol, phosphatidyl serine, phosphatidic acid, 2-lysophosphatidyl choline, and a sphingomyelin.

[0695] A fatty acid moiety can be selected, for example, from the non-limiting group consisting of lauric acid, myristic acid, myristoleic acid, palmitic acid, palmitoleic acid, stearic acid, oleic acid, linoleic acid, alpha-linolenic acid, erucic acid, phytanoic acid, arachidic acid, arachidonic acid, eicosapentaenoic acid, behenic acid, docosapentaenoic acid, and docosahexaenoic acid.

[0696] Particular phospholipids can facilitate fusion to a membrane. In some embodiments, a cationic phospholipid can interact with one or more negatively charged phospholipids of a membrane (e.g., a cellular or intracellular membrane). Fusion of a phospholipid to a membrane can allow one or more elements (e.g., a therapeutic agent) of a lipid-containing composition (e.g., LNPs) to pass through the membrane permitting, e.g., delivery of the one or more elements to a target tissue.

[0697] Non-natural phospholipid species including natural species with modifications and substitutions including branching, oxidation, cyclization, and alkynes are also contemplated. In some embodiments, a phospholipid can be functionalized with or cross-linked to one or more alkynes (e.g., an alkenyl group in which one or more double bonds is replaced with a triple bond). Under appropriate reaction conditions, an alkyne group can undergo a copper-catalyzed cycloaddition upon exposure to an azide. Such reactions can be useful in functionalizing a lipid bilayer of a nanoparticle composition to facilitate membrane permeation or cellular recognitionor in conjugating a nanoparticle composition to a useful component such as a targeting or imaging moiety (e.g., a dye).

[0698] Phospholipids include, but are not limited to, glycerophospholipids such as phosphatidylcholines, phosphatidylethanolamines, phosphatidylserines, phosphatidylinositols, phosphatidy glycerols, and phosphatidic acids. Phospholipids also include phosphosphingolipid, such as sphingomyelin.

[0699] In some embodiments, a phospholipid useful or potentially useful in the present invention is an analog or variant of DSPC. In some embodiments, a phospholipid useful or potentially useful in the present invention is a compound of Formula (PL-I):or a salt thereof, wherein: each R1is independently optionally substituted alkyl; or optionally two R1are joined together with the intervening atoms to form optionally substituted monocyclic carbocyclyl or optionally substituted monocyclic heterocyclyl; or optionally three R1are joined together with the intervening atoms to form optionally substituted bicyclic carbocyclyl or optionally substitute bicyclic heterocyclyl; n is 1, 2, 3, 4, 5, 6, 7, 8, 9, or 10; m is 0, 1, 2, 3, 4, 5, 6, 7, 8, 9, or 10;A is of the formula:each instance of L2is independently a bond or optionally substituted Ci-6 alkylene, wherein one methylene unit of the optionally substituted Ci-6 alkylene is optionally replaced with -O-, -N(RN)-, -S-, -C(O)-, -C(O)N(RN)-, -NRNC(O)-, -C(O)O-, -OC(O)-, -OC(O)O-, -OC(O)N(RN)-, -NRNC(O)O-, or -NRNC(O)N(RN)-; each instance of R2is independently optionally substituted C1-30 alkyl, optionally substituted C1-30 alkenyl, or optionally substituted C1-30 alkynyl; optionally wherein one or more methylene units of R2are independently replaced with optionally substituted carbocyclylene, optionally substituted heterocyclylene, optionally substituted arylene, optionally substituted heteroarylene, -N(RN)-, -O-, -S-, -C(O)-, -C(O)N(RN)-, -NRNC(O)-, -NRNC(O)N(RN)-, -C(O)O-, -OC(O)-, -OC(O)O-, -OC(O)N(RN)-, -NRNC(O)O-, -C(O)S-, -SC(O)-, -C(=NRN)-, -C(=NRN)N(RN)-, -NRNC(=NRN)-, -NRNC(=NRN)N(RN)-, -C(S)-,-C(S)N(RN)-, -NRNC(S)-, -NRNC(S)N(RN)-, -S(O)-, -OS(O)-, -S(O)O-, -OS(O)O-, -OS(O)2-, -S(O)2O-, -OS(O)2O-, -N(RN)S(O)-, -S(O)N(RN)-, -N(RN)S(O)N(RN)-, -OS(O)N(RN)-, -N(RN)S(O)O-, -S(O)2-, -N(RN)S(O)2-, -S(O)2N(RN)-, -N(RN)S(O)2N(RN)-, -OS(O)2N(RN)-, or -N(RN)S(O)2O-; each instance of RNis independently hydrogen, optionally substituted alkyl, or a nitrogen protecting group;Ring B is optionally substituted carbocyclyl, optionally substituted heterocyclyl, optionally substituted aryl, or optionally substituted heteroaryl; and p is 1 or 2; provided that the compound is not of the formula:wherein each instance of R2is independently unsubstituted alkyl, unsubstituted alkenyl, or unsubstituted alkynyl.

[0700] In some embodiments, the phospholipids may be one or more of the phospholipids described in U.S. Application No. 62 / 520,530.

[0701] In some embodiments, the phospholipids may be selected from the non-limiting group consisting of l,2-distearoyl-sn-glycero-3-phosphocholine (DSPC), l,2-dioleoyl-sn-glycero-3- phosphoethanolamine (DOPE), l,2-dilinoleoyl-sn-glycero-3 -phosphocholine (DLPC), 1,2- dimyristoyl-sn-glycero-phosphocholine (DMPC), l,2-dioleoyl-sn-glycero-3 -phosphocholine (DOPC), l,2-dipalmitoyl-sn-glycero-3 -phosphocholine (DPPC), 1,2-diundecanoyl-sn- glycero-phosphocholine (DUPC), l-palmitoyl-2-oleoyl-sn-glycero-3 -phosphocholine(POPC), l,2-di-O-octadecenyl- w-glycero-3 -phosphocholine (18:0 Diether PC), l-oleoyl-2- cholesterylhemisuccinoyl-sw-glycero-3-phosphocholine (OChemsPC), 1-hexadecyl-sn- glycero-3 -phosphocholine (C16 Lyso PC), l,2-dilinolenoyl-sn-glycero-3 -phosphocholine, 1,2- diarachidonoyl-sn-glycero-3 -phosphocholine, l,2-didocosahexaenoyl-sn-glycero-3- phosphocholine, l,2-diphytanoyl-sn-glycero-3 -phosphoethanolamine (ME 16.0 PE), 1,2- distearoyl-sn-glycero-3-phosphoethanolamine, l,2-dilinoleoyl-sn-glycero-3- phosphoethanolamine, 1 ,2-dilinolenoyl-sn-glycero-3 -phosphoethanolamine, 1 ,2- diarachidonoyl-sn-glycero-3 -phosphoethanolamine, l,2-didocosahexaenoyl-sn-glycero-3- phosphoethanolamine, l,2-dioleoyl-sn-glycero-3-phospho-rac-(l -glycerol) sodium salt(DOPG), and sphingomyelin. In some embodiments, a LNP includes DSPC. In some embodiments, a LNP includes DOPE. In some embodiments, a LNP includes both DSPC and DOPE. i) Phospholipid Head Modifications

[0702] In some embodiments, a phospholipid useful or potentially useful in the present invention comprises a modified phospholipid head (e.g., a modified choline group). In some embodiments, a phospholipid with a modified head is DSPC, or analog thereof, with a modified quaternary amine. In some embodiments, in embodiments of Formula (PL-I), at least one of R1is not methyl. In some embodiments, at least one of R1is not hydrogen or methyl. In some embodiments, the compound of Formula (PL-I) is one of the following formulae:or a salt thereof, wherein: each t is independently 1, 2, 3, 4, 5, 6, 7, 8, 9, or 10; each u is independently 0, 1, 2, 3, 4, 5, 6, 7, 8, 9, or 10; and each v is independently 1, 2, or 3.In some embodiments, a compound of Formula (PL-I) is of Formula (PL-I-a):or a salt thereof.

[0703] In some embodiments, a phospholipid useful or potentially useful in the present invention comprises a cyclic moiety in place of the glyceride moiety. In some embodiments, a phospholipid useful in the present invention is DSPC, or analog thereof, with a cyclic moiety in place of the glyceride moiety. In some embodiments, the compound of Formula (PL-I) is of Formula (PL-I-b):or a salt thereof. ii) Phospholipid Tail Modifications

[0704] In some embodiments, a phospholipid useful or potentially useful in the present invention comprises a modified tail. In some embodiments, a phospholipid useful or potentially useful in the present invention is DSPC, or analog thereof, with a modified tail. As described herein, a “modified tail” may be a tail with shorter or longer aliphatic chains, aliphatic chains with branching introduced, aliphatic chains with substituents introduced, aliphatic chains wherein one or more methylenes are replaced by cyclic or heteroatom groups, or any combination thereof. In some embodiments, In some embodiments, the compound of (PL-I) is of Formula (PL-I-a), or a salt thereof, wherein at least one instance of R2is each instance of R2is optionally substituted C1-30 alkyl, wherein one or more methylene units of R2are independently replaced with optionally substituted carbocyclylene, optionally substituted heterocyclylene, optionally substituted arylene, optionally substituted heteroarylene, -N(RN)-,-O-, -S-, -C(O)-, -C(O)N(RN)-, -NRNC(O)-, -NRNC(O)N(RN)-, -C(O)O-, -OC(O)-, -OC(O)O-, -OC(O)N(RN)-, -NRNC(O)O-, -C(O)S-, -SC(O)-, -C(=NRN)-, -C(=NRN)N(RN)-,-NRNC(=NRN)-, -NRNC(=NRN)N(RN)-, -C(S)-, -C(S)N(RN)-, -NRNC(S)-, -NRNC(S)N(RN)-, -S(O)-, -OS(O)-, -S(O)O-, -OS(O)O-, -OS(O)2-, -S(O)2O-, -OS(O)2O-, -N(RN)S(O)-, -S(O)N(RN)-, -N(RN)S(O)N(RN)-, -OS(O)N(RN)-, -N(RN)S(O)O-, -S(O)2-, -N(RN)S(O)2-, -S(O)2N(RN)-, -N(RN)S(O)2N(RN)-, -OS(O)2N(RN)-, or -N(RN)S(O)2O-.

[0705] In some embodiments, the compound of Formula (PL-I) is of Formula (PL-I-c):or a salt thereof, wherein: each x is independently an integer between 0-30, inclusive; and each instance is G is independently selected from the group consisting of optionally substituted carbocyclylene, optionally substituted heterocyclylene, optionally substituted arylene, optionally substituted heteroarylene, -N(RN)-, -O-, -S-, -C(O)-, -C(O)N(RN)-, -NRNC(O)-, -NRNC(O)N(RN)-, -C(O)O-, -OC(O)-, -OC(O)O-, -OC(O)N(RN)-, -NRNC(O)O-,-C(O)S-, -SC(O)-, -C(=NRN)-, -C(=NRN)N(RN)-, -NRNC(=NRN)-, -NRNC(=NRN)N(RN)-, -C(S)-, -C(S)N(RN)-, -NRNC(S)-, -NRNC(S)N(RN)-, -S(O)-, -OS(O)-, -S(O)O-, -OS(O)O-, -OS(O)2-, -S(O)2O-, -OS(O)2O-, -N(RN)S(O)-, -S(O)N(RN)-, -N(RN)S(O)N(RN)-, -OS(O)N(RN)-, -N(RN)S(O)O-, -S(O)2-, -N(RN)S(O)2-, -S(O)2N(RN)-, -N(RN)S(O)2N(RN)-, -OS(O)2N(RN)-, or -N(RN)S(O)2O-. Each possibility represents a separate embodiment of the present invention.

[0706] In some embodiments, a phospholipid useful or potentially useful in the present invention comprises a modified phosphocholine moiety, wherein the alkyl chain linking the quaternary amine to the phosphoryl group is not ethylene (e.g., n is not 2). Therefore, in some embodiments, a phospholipid useful or potentially useful in the present invention is a compound of Formula (PL-I), wherein n is 1, 3, 4, 5, 6, 7, 8, 9, or 10. In some embodiments, a compound of Formula (PL-I) is of one of the following formulae:or a salt thereof.Alternative lipids

[0707] In some embodiments, an alternative lipid is used in place of a phospholipid of the present disclosure. Non-limiting examples of such alternative lipids include the following:Therapeutic Agents

[0708] Lipid nanoparticles (e.g., empty LNPs or loaded LNPs) may include one or more therapeutic and / or prophylactics. The disclosure features methods of delivering a therapeutic and / or prophylactic to a mammalian cell or organ, producing a polypeptide of interest in a mammalian cell, and treating a disease or disorder in a mammal in need thereof comprising administering to a mammal and / or contacting a mammalian cell with a lipid nanoparticle (e.g., an empty LNP or a loaded LNP) including a therapeutic and / or prophylactic.

[0709] Therapeutic and / or prophylactics include biologically active substances and are alternately referred to as “active agents.” A therapeutic and / or prophylactic may be a substance that, once delivered to a cell or organ, brings about a desirable change in the cell, organ, or other bodily tissue or system. Such species may be useful in the treatment of one or more diseases, disorders, or conditions. In some embodiments, a therapeutic and / or prophylactic is a small molecule drug useful in the treatment of a particular disease, disorder, or condition.

[0710] In some embodiments, a therapeutic and / or prophylactic is a vaccine, a compound (e.g., a polynucleotide or nucleic acid molecule that encodes a protein or polypeptide or peptide or aprotein or polypeptide or protein) that elicits an immune response, and / or another therapeutic and / or prophylactic. Vaccines include compounds and preparations that are capable of providing immunity against one or more conditions related to infectious diseases and can include mRNAs encoding infectious disease derived antigens and / or epitopes. Vaccines also include compounds and preparations that direct an immune response against cancer cells and can include mRNAs encoding tumor cell derived antigens, epitopes, and / or neoepitopes. In some embodiments, a vaccine and / or a compound capable of eliciting an immune response is administered intramuscularly via a composition of the disclosure.

[0711] In other embodiments, a therapeutic and / or prophylactic is a protein, for example a protein needed to augment or replace a naturally-occurring protein of interest. Such proteins or polypeptides may be naturally occurring, or may be modified using methods known in the art, e.g., to increase half life. Exemplary proteins are intracellular, transmembrane, or secreted.Polynucleotides and nucleic acids

[0712] In some embodiments, the therapeutic agent is an agent that enhances (i.e., increases, stimulates, upregulates) protein expression. Non-limiting examples of types of therapeutic agents that can be used for enhancing protein expression include RNAs, mRNAs, dsRNAs, CRISPR / Cas9 technology, ssDNAs and DNAs (e.g., expression vectors). The agent that upregulates protein expression may upregulate expression of a naturally occurring or non- naturally occurring protein (e.g., a chimeric protein that has been modified to improve half life, or one that comprises desirable amino acid changes). Exemplary proteins include intracellular, transmembrane, or secreted proteins, peptides, or polypeptides.

[0713] In some embodiments, the therapeutic agent is a DNA therapeutic agent. The DNA molecule can be a double-stranded DNA, a single-stranded DNA (ssDNA), or a molecule that is a partially double-stranded DNA, i.e., has a portion that is double-stranded and a portion that is single-stranded. In some cases the DNA molecule is triple-stranded or is partially triplestranded, i.e., has a portion that is triple stranded and a portion that is double stranded. The DNA molecule can be a circular DNA molecule or a linear DNA molecule.

[0714] A DNA therapeutic agent can be a DNA molecule that is capable of transferring a gene into a cell, e.g., that encodes and can express a transcript. In other embodiments, the DNA molecule is a synthetic molecule, e.g., a synthetic DNA molecule produced in vitro. In some embodiments, the DNA molecule is a recombinant molecule. Non-limiting exemplary DNA therapeutic agents include plasmid expression vectors and viral expression vectors.

[0715] The DNA therapeutic agents described herein, e.g., DNA vectors, can include a variety of different features. The DNA therapeutic agents described herein, e.g., DNA vectors, can include a non-coding DNA sequence. For example, a DNA sequence can include at least one regulatory element for a gene, e.g., a promoter, enhancer, termination element, polyadenylation signal element, splicing signal element, and the like. In some embodiments, the non-coding DNA sequence is an intron. In some embodiments, the non-coding DNA sequence is a transposon. In some embodiments, a DNA sequence described herein can have a non-coding DNA sequence that is operatively linked to a gene that is transcriptionally active. In other embodiments, a DNA sequence described herein can have a non-coding DNA sequence that is not linked to a gene, i.e., the non-coding DNA does not regulate a gene on the DNA sequence.

[0716] In some embodiments, in the loaded LNP of the disclosure, the one or more therapeutic and / or prophylactic agents is a nucleic acid. In some embodiments, the one or more therapeutic and / or prophylactic agents is selected from the group consisting of a ribonucleic acid (RNA) and a deoxyribonucleic acid (DNA).

[0717] For example, in some embodiments, when the therapeutic and / or prophylactic agents is a DNA, the DNA is selected from the group consisting of a double-stranded DNA, a singlestranded DNA (ssDNA), a partially double-stranded DNA, a triple stranded DNA, and a partially triple-stranded DNA. In some embodiments, the DNA is selected from the group consisting of a circular DNA, a linear DNA, and mixtures thereof.

[0718] In some embodiments, in the loaded LNP of the disclosure, the one or more therapeutic and / or prophylactic agents is selected from the group consisting of a plasmid expression vector, a viral expression vector, and mixtures thereof.

[0719] For example, in some embodiments, when the therapeutic and / or prophylactic agents is a RNA, the RNA is selected from the group consisting of a single-stranded RNA, a doublestranded RNA (dsRNA), a partially double-stranded RNA, and mixtures thereof. In some embodiments, the RNA is selected from the group consisting of a circular RNA, a linear RNA, and mixtures thereof.

[0720] For example, in some embodiments, when the therapeutic and / or prophylactic agents is a RNA, the RNA is selected from the group consisting of a short interfering RNA (siRNA), an asymmetrical interfering RNA (aiRNA), a RNA interference (RNAi) molecule, a microRNA (miRNA), an antagomir, an antisense RNA, a ribozyme, a Dicer-substrate RNA (dsRNA), a small hairpin RNA (shRNA), a messenger RNA (mRNA), locked nucleic acids (LNAs) and CRISPR / Cas9 technology, and mixtures thereof.

[0721] For example, in some embodiments, when the therapeutic and / or prophylactic agents is a RNA, the RNA is selected from the group consisting of a small interfering RNA (siRNA), an asymmetrical interfering RNA (aiRNA), a microRNA (miRNA), a Dicer-substrate RNA (dsRNA), a small hairpin RNA (shRNA), a messenger RNA (mRNA), and mixtures thereof.

[0722] In some embodiments, the one or more therapeutic and / or prophylactic agents is an mRNA. In some embodiments, the one or more therapeutic and / or prophylactic agents is a modified mRNA (mmRNA).

[0723] In some embodiments, the one or more therapeutic and / or prophylactic agents is an mRNA that incorporates a micro-RNA binding site (miR binding site). Further, in some embodiments, an mRNA includes one or more of a stem loop, a chain terminating nucleoside, a polyA sequence, a polyadenylation signal, and / or a 5’ cap structure.

[0724] An mRNA may be a naturally or non-naturally occurring mRNA. An mRNA may include one or more modified nucleobases, nucleosides, or nucleotides, as described below, in which case it may be referred to as a “modified mRNA” or “mmRNA.” As described herein “nucleoside” is defined as a compound containing a sugar molecule (e.g., a pentose or ribose) or derivative thereof in combination with an organic base (e.g., a purine or pyrimidine) or a derivative thereof (also referred to herein as “nucleobase”). As described herein, “nucleotide” is defined as a nucleoside including a phosphate group.

[0725] An mRNA may include a 5' untranslated region (5'-UTR), a 3' untranslated region (3'- UTR), and / or a coding region (e.g., an open reading frame). An mRNA may include any suitable number of base pairs, including tens (e.g., 10, 20, 30, 40, 50, 60, 70, 80, 90 or 100), hundreds (e.g., 200, 300, 400, 500, 600, 700, 800, or 900) or thousands (e.g., 1000, 2000, 3000, 4000, 5000, 6000, 7000, 8000, 9000, 10,000) of base pairs. Any number (e.g., all, some, or none) of nucleobases, nucleosides, or nucleotides may be an analog of a canonical species, substituted, modified, or otherwise non-naturally occurring. In certain embodiments, all of a particular nucleobase type may be modified. In some embodiments, all uracils or uridines are modified. When all nucleobases, nucleosides, or nucleotides are modified, e.g., all uracils or uridines, the mRNA can be referred to as “fully modified”, e.g., for uracil or uridine.

[0726] In some embodiments, an mRNA as described herein may include a 5' cap structure, a chain terminating nucleotide, optionally a Kozak sequence (also known as a Kozak consensus sequence), a stem loop, a polyA sequence, and / or a polyadenylation signal.

[0727] A 5' cap structure or cap species is a compound including two nucleoside moi eties joined by a linker and may be selected from a naturally occurring cap, a non-naturally occurring cap or cap analog, or an anti-reverse cap analog (ARCA). A cap species may include one ormore modified nucleosides and / or linker moieties. For example, a natural mRNA cap may include a guanine nucleotide and a guanine (G) nucleotide methylated at the 7 position joined by a triphosphate linkage at their 5' positions, e.g., m7G(5')ppp(5')G, commonly written as m7GpppG. A cap species may also be an anti-reverse cap analog. A non-limiting list of possible cap species includes m7GpppG, m7Gpppm7G, m73'dGpppG, m27,O3'GpppG, m27,O3'GppppG, m27,O2'GppppG, m7Gpppm7G, m73'dGpppG, m27,O3'GpppG, m27,O3'GppppG, and m27,O2'GppppG.

[0728] An mRNA may instead or additionally include a chain terminating nucleoside. For example, a chain terminating nucleoside may include those nucleosides deoxygenated at the 2’ and / or 3' positions of their sugar group. Such species may include 3' deoxyadenosine (cordycepin), 3' deoxyuridine, 3' deoxy cytosine, 3' deoxyguanosine, 3' deoxythymine, and 2', 3' dideoxynucleosides, such as 2', 3' dideoxyadenosine, 2', 3' dideoxyuridine, 2', 3' dideoxy cytosine, 2', 3' dideoxyguanosine, and 2', 3' dideoxythymine. In some embodiments, incorporation of a chain terminating nucleotide into an mRNA, for example at the 3 '-terminus, may result in stabilization of the mRNA.

[0729] An mRNA may instead or additionally include a stem loop, such as a histone stem loop. A stem loop may include 2, 3, 4, 5, 6, 7, 8, or more nucleotide base pairs. For example, a stem loop may include 4, 5, 6, 7, or 8 nucleotide base pairs. A stem loop may be located in any region of an mRNA. For example, a stem loop may be located in, before, or after an untranslated region (a 5' untranslated region or a 3' untranslated region), a coding region, or a poly A sequence or tail. In some embodiments, a stem loop may affect one or more function(s) of an mRNA, such as initiation of translation, translation efficiency, and / or transcriptional termination.

[0730] An mRNA may instead or additionally include a polyA sequence and / or polyadenylation signal. A polyA sequence may be comprised entirely or mostly of adenine nucleotides or analogs or derivatives thereof. A poly A sequence may also comprise stabilizing nucleotides or analogs. For example, a poly A sequence can include deoxythymidine, e.g., inverted (or reverse linkage) deoxythymidine (dT), as a stabilizing nucleotide or analog. Detials on using inverted dT and other stabilizing poly A sequence modifications can be found, for example, in WO2017 / 049275 A2, the content of which is incoported herein by reference. A polyA sequence may be a tail located adjacent to a 3' untranslated region of an mRNA. In some embodiments, a polyA sequence may affect the nuclear export, translation, and / or stability of an mRNA.

[0731] An mRNA may instead or additionally include a microRNA binding site. MicroRNA binding sites (or miR binding sites) can be used to regulate mRNA expression in various tissues or cell types. In exemplary embodiments, miR binding sites are engineered into 3’ UTR sequences of an mRNA to regulate, e.g., enhance degradation of mRNA in cells or tissues expressing the cognate miR. Such regulation is useful to regulate or control “off-target” expression ir mRNAs, z.e., expression in undesired cells or tissues in vivo. Detials on using mir binding sites can be found, for example, in WO 2017 / 062513 A2, the content of which is incoported herein by reference.

[0732] In some embodiments, an mRNA is a bicistronic mRNA comprising a first coding region and a second coding region with an intervening sequence comprising an internal ribosome entry site (IRES) sequence that allows for internal translation initiation between the first and second coding regions, or with an intervening sequence encoding a self-cleaving peptide, such as a 2A peptide. IRES sequences and 2A peptides are typically used to enhance expression of multiple proteins from the same vector. A variety of IRES sequences are known and available in the art and may be used, including, e.g., the encephalomyocarditis virus IRES.

[0733] In some embodiments, an mRNA of the disclosure comprises one or more modified nucleobases, nucleosides, or nucleotides (termed “modified mRNAs” or “mmRNAs”). In some embodiments, modified mRNAs may have useful properties, including enhanced stability, intracellular retention, enhanced translation, and / or the lack of a substantial induction of the innate immune response of a cell into which the mRNA is introduced, as compared to a reference unmodified mRNA. Therefore, use of modified mRNAs may enhance the efficiency of protein production, intracellular retention of nucleic acids, as well as possess reduced immunogenicity.

[0734] In some embodiments, an mRNA includes one or more (e.g., 1, 2, 3 or 4) different modified nucleobases, nucleosides, or nucleotides. In some embodiments, an mRNA includes one or more (e.g., 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 20, 30, 40, 50, 60, 70, 80, 90, 100, or more) different modified nucleobases, nucleosides, or nucleotides. In some embodiments, the modified mRNA may have reduced degradation in a cell into which the mRNA is introduced, relative to a corresponding unmodified mRNA.

[0735] In some embodiments, the modified nucleobase is a modified uracil. Exemplary nucleobases and nucleosides having a modified uracil include pseudouridine (y), pyridin-4- one ribonucleoside, 5-aza-uridine, 6-aza-uridine, 2-thio-5-aza-uridine, 2-thio-uridine (s2U), 4- thio-uridine (s4U), 4-thio-pseudouridine, 2-thio-pseudouridine, 5-hydroxy-uridine (ho5U), 5- aminoallyl-uridine, 5-halo-uridine (e.g., 5-iodo-uridineor 5 -bromo-uridine), 3 -methyl -uridine(m3U), 5-methoxy-uridine (mo5U), uridine 5-oxyacetic acid (cmo5U), uridine 5-oxyacetic acid methyl ester (mcmo5U), 5-carboxymethyl-uridine (cm5U), 1 -carboxymethylpseudouridine, 5-carboxyhydroxymethyl-uridine (chm5U), 5-carboxyhydroxymethyl-uridine methyl ester (mchm5U), 5-methoxycarbonylmethyl-uridine (mcm5U), 5- methoxycarbonylmethyl-2-thio-uridine (mcm5s2U), 5 -aminomethyl -2 -thio-uridine (nm5s2U), 5-methylaminomethyl-uridine (mnm5U), 5-methylaminomethyl-2-thio-uridine (mnm5s2U), 5-methylaminomethyl-2-seleno-uridine (mnm5se2U), 5-carbamoylmethyl-uridine (ncm5U), 5-carboxymethylaminomethyl -uridine (cmnm5U), 5-carboxymethylaminomethyl -2 -thiouridine (cmnm5s2U), 5-propynyl-uridine, 1-propynyl-pseudouridine, 5 -taurinom ethyl -uridine (rm5U), 1 -taurinom ethyl -pseudouridine, 5-taurinomethyl-2-thio-uridine(Tm5s2U), 1- taurinomethyl-4-thio-pseudouridine, 5 -methyl -uridine (m5U, i.e., having the nucleobase deoxythymine), 1-methyl-pseudouridine (mly), 5-methyl-2-thio-uridine (m5s2U), 1-methyl- 4-thio-pseudouridine (mls4y), 4-thio-l-methyl-pseudouridine, 3-methyl-pseudouridine (m3y), 2-thio- 1-methyl-pseudouridine, 1 -methyl- 1-deaza-pseudouri dine, 2-thio-l-methyl-l- deaza-pseudouridine, dihydrouridine (D), dihydropseudouridine, 5,6-dihydrouridine, 5- methyl-dihydrouridine (m5D), 2-thio-dihydrouridine, 2-thio-dihydropseudouridine, 2- methoxy-uridine, 2-methoxy-4-thio-uridine, 4-methoxy-pseudouridine, 4-methoxy-2-thio- pseudouridine, N1 -methyl -pseudouridine, 3-(3-amino-3-carboxypropyl)uridine (acp3U), 1- methyl-3-(3-amino-3-carboxypropyl)pseudouridine (acp3 y), 5-(isopentenylaminomethyl)uridine (inm5U), 5-(isopentenylaminomethyl)-2 -thio-uridine (inm5s2U), a-thio-uridine, 2'-O-methyl-uridine (Um), 5,2'-O-dimethyl-uridine (m5Um), 2'-O- methyl-pseudouridine (ym), 2-thio-2'-O-methyl-uridine (s2Um), 5-methoxycarbonylmethyl- 2'-O-methyl-uridine (mcm5Um), 5-carbamoylmethyl-2'-O-methyl-uridine (ncm5Um), 5- carboxymethylaminomethyl-2'-O-methyl -uridine (cmnm5Um), 3, 2'-O-dimethyl -uridine (m3Um), and 5-(isopentenylaminomethyl)-2'-O-methyl-uridine (inm5Um), 1 -thio-uridine, deoxythymidine, 2’-F-ara-uridine, 2’-F-uridine, 2’-OH-ara-uridine, 5-(2-carbomethoxyvinyl) uridine, and 5-[3-(l-E-propenylamino)]uridine.

[0736] In some embodiments, the modified nucleobase is a modified cytosine. Exemplary nucleobases and nucleosides having a modified cytosine include 5 -aza-cytidine, 6-aza- cytidine, pseudoisocytidine, 3-methyl-cytidine (m3C), N4-acetyl-cytidine (ac4C), 5-formyl- cytidine (f5C), N4-methyl-cytidine (m4C), 5-methyl-cytidine (m5C), 5-halo-cytidine (e.g., 5- iodo-cytidine), 5 -hydroxymethyl -cytidine (hm5C), 1 -methyl -pseudoisocytidine, pyrrolo- cytidine, pyrrolo-pseudoisocytidine, 2-thio-cytidine (s2C), 2-thio-5-methyl-cytidine, 4-thio- pseudoisocytidine, 4-thio-l -methyl -pseudoisocytidine, 4-thio-l-methyl-l-deaza-pseudoisocytidine, 1 -methyl- 1-deaza-pseudoisocyti dine, zebularine, 5-aza-zebularine, 5- methyl-zebularine, 5-aza-2-thio-zebularine, 2-thio-zebularine, 2-methoxy-cytidine, 2- methoxy-5-methyl-cytidine, 4-methoxy-pseudoisocytidine, 4-methoxy-l -methyl - pseudoisocytidine, lysidine (k2C), a-thio-cytidine, 2'-O-methyl-cytidine (Cm), 5,2'-O- dimethyl-cytidine (m5Cm), N4-acetyl-2'-O-methyl-cytidine (ac4Cm), N4,2'-O-dimethyl- cytidine (m4Cm), 5-formyl-2'-O-methyl-cytidine (f5Cm), N4,N4,2'-O-trimethyl-cytidine (m42Cm), 1 -thio-cytidine, 2’-F-ara-cytidine, 2’-F-cytidine, and 2’-OH-ara-cytidine.

[0737] In some embodiments, the modified nucleobase is a modified adenine. Exemplary nucleobases and nucleosides having a modified adenine include a-thio-adenosine, 2-amino- purine, 2, 6-diaminopurine, 2-amino-6-halo-purine (e.g., 2-amino-6-chloro-purine), 6-halo- purine (e.g., 6-chloro-purine), 2-amino-6-methyl-purine, 8-azido-adenosine, 7-deaza-adenine, 7-deaza-8-aza-adenine, 7-deaza-2-amino-purine, 7-deaza-8-aza-2-amino-purine, 7-deaza-2,6- diaminopurine, 7-deaza-8-aza-2, 6-diaminopurine, 1 -methyl -adenosine (mlA), 2-methyl- adenine (m2A), N6-methyl-adenosine (m6A), 2-methylthio-N6-methyl-adenosine (ms2m6A), N6-isopentenyl-adenosine (i6A), 2-methylthio-N6-isopentenyl-adenosine (ms2i6A), N6-(cis- hydroxyisopentenyl)adenosine (io6A), 2-methylthio-N6-(cis-hydroxyisopentenyl)adenosine (ms2io6A), N6-glycinylcarbamoyl-adenosine (g6A), N6-threonylcarbamoyl-adenosine (t6A), N6-methyl-N6-threonylcarbamoyl -adenosine (m6t6A), 2-methylthio-N6-threonylcarbamoyl- adenosine (ms2g6A), N6,N6-dimethyl-adenosine (m62A), N6-hydroxynorvalylcarbamoyl- adenosine (hn6A), 2-methylthio-N6-hydroxynorvalylcarbamoyl-adenosine (ms2hn6A), N6- acetyl-adenosine (ac6A), 7-methyl-adenine, 2-methylthio-adenine, 2-methoxy-adenine, a- thio-adenosine, 2 '-O-m ethyl -adenosine (Am), N6,2'-O-dimethyl-adenosine (m6Am), N6,N6,2'-O-trimethyl-adenosine (m62Am), l,2'-O-dimethyl-adenosine (mlAm), 2'-O- ribosyladenosine (phosphate) (Ar(p)), 2-amino-N6-methyl-purine, 1 -thio-adenosine, 8-azido- adenosine, 2’-F-ara-adenosine, 2’-F-adenosine, 2’-OH-ara-adenosine, and N6-(19-amino- pentaoxanonadecyl)-adenosine.

[0738] In some embodiments, the modified nucleobase is a modified guanine. Exemplary nucleobases and nucleosides having a modified guanine include a-thio-guanosine, inosine (I), 1 -methyl -inosine (mil), wyosine (imG), methyl wyosine (mimG), 4-dem ethyl -wyosine (imG- 14), isowyosine (imG2), wybutosine (yW), peroxy wybutosine (o2yW), hydroxy wybutosine (OhyW), undermodified hydroxywybutosine (OhyW*), 7-deaza-guanosine, queuosine (Q), epoxyqueuosine (oQ), galactosyl-queuosine (galQ), mannosyl-queuosine (manQ), 7-cyano-7- deaza-guanosine (preQO), 7-aminom ethyl -7-deaza-guanosine (preQi), archaeosine (G+), 7- deaza-8-aza-guanosine, 6-thio-guanosine, 6-thio-7-deaza-guanosine, 6-thio-7-deaza-8-aza-guanosine, 7-methyl -guanosine (m7G), 6-thio-7-methyl-guanosine, 7-methyl -inosine, 6- methoxy-guanosine, 1 -methyl -guanosine (mlG), N2-methyl-guanosine (m2G), N2,N2- dimethyl-guanosine (m22G), N2,7-dimethyl-guanosine (m2,7G), N2, N2,7-dimethyl- guanosine (m2,2,7G), 8 -oxo-guanosine, 7-methyl-8-oxo-guanosine, l-methyl-6-thio- guanosine, N2-methyl-6-thio-guanosine, N2,N2-dimethyl-6-thio-guanosine, a-thio-guanosine, 2'-O-methyl-guanosine (Gm), N2-methyl-2'-O-methyl-guanosine (m2Gm), N2,N2-dimethyl- 2'-O-methyl-guanosine (m22Gm), l-methyl-2'-O-methyl-guanosine (ml Gm), N2,7-dimethyl- 2'-O-methyl-guanosine (m2,7Gm), 2'-O-methyl-inosine (Im), l,2'-O-dimethyl-inosine (mllm), 2'-O-ribosylguanosine (phosphate) (Gr(p)) , 1 -thio-guanosine, O6-methyl-guanosine, 2’-F-ara-guanosine, and 2’-F-guanosine.

[0739] In some embodiments, an mRNA of the disclosure includes a combination of one or more of the aforementioned modified nucleobases (e.g., a combination of 2, 3 or 4 of the aforementioned modified nucleobases.)

[0740] In some embodiments, the modified nucleobase is pseudouridine (y), Nl- methylpseudouridine (mly), 2-thiouridine, 4’ -thiouridine, 5-methylcytosine, 2-thio-l-methyl- 1-deaza-pseudouridine, 2-thio-l-methyl-pseudouridine, 2-thio-5-aza-uridine , 2-thio- dihydropseudouridine, 2-thio-dihydrouridine, 2-thio-pseudouridine, 4-methoxy-2-thio- pseudouridine, 4-methoxy-pseudouridine, 4-thio-l-methyl-pseudouridine, 4-thio- pseudouridine, 5-aza-uridine, dihydropseudouridine, 5-methoxyuridine, or 2’-O-methyl uridine. In some embodiments, an mRNA of the disclosure includes a combination of one or more of the aforementioned modified nucleobases (e.g., a combination of 2, 3 or 4 of the aforementioned modified nucleobases.) In some embodiments, the modified nucleobase isNl- methylpseudouridine (mly) and the mRNA of the disclosure is fully modified with Nl- methylpseudouridine (mly). In some embodiments, N1 -methylpseudouridine (m h| / ) represents from 75-100% of the uracils in the mRNA. In some embodiments, Nl- methylpseudouridine (m h| / ) represents 100% of the uracils in the mRNA.

[0741] In some embodiments, the modified nucleobase is a modified cytosine. Exemplary nucleobases and nucleosides having a modified cytosine include N4-acetyl-cytidine (ac4C), 5- methyl-cytidine (m5C), 5-halo-cytidine (e.g., 5-iodo-cytidine), 5-hydroxymethyl-cytidine (hm5C), 1-methyl-pseudoisocytidine, 2-thio-cytidine (s2C), 2-thio-5-methyl-cytidine. In some embodiments, an mRNA of the disclosure includes a combination of one or more of the aforementioned modified nucleobases (e.g., a combination of 2, 3 or 4 of the aforementioned modified nucleobases.)

[0742] In some embodiments, the modified nucleobase is a modified adenine. Exemplary nucleobases and nucleosides having a modified adenine include 7-deaza-adenine, 1 -methyladenosine (ml A), 2-methyl-adenine (m2 A), N6-methyl-adenosine (m6A). In some embodiments, an mRNA of the disclosure includes a combination of one or more of the aforementioned modified nucleobases (e.g., a combination of 2, 3 or 4 of the aforementioned modified nucleobases.)

[0743] In some embodiments, the modified nucleobase is a modified guanine. Exemplary nucleobases and nucleosides having a modified guanine include inosine (I), 1-methyl-inosine (mil), wyosine (imG), methyl wyosine (mimG), 7-deaza-guanosine, 7-cyano-7-deaza- guanosine (preQO), 7-aminomethyl-7-deaza-guanosine (preQi), 7-methyl-guanosine (m7G), 1 -methyl -guanosine (mlG), 8-oxo-guanosine, 7-methyl-8-oxo-guanosine. In some embodiments, an mRNA of the disclosure includes a combination of one or more of the aforementioned modified nucleobases (e.g., a combination of 2, 3 or 4 of the aforementioned modified nucleobases.)

[0744] In some embodiments, the modified nucleobase is 1 -methyl -pseudouridine (mly), 5- methoxy-uridine (mo5U), 5-methyl-cytidine (m5C), pseudouridine (y), a-thio-guanosine, or a-thio-adenosine. In some embodiments, an mRNA of the disclosure includes a combination of one or more of the aforementioned modified nucleobases (e.g., a combination of 2, 3 or 4 of the aforementioned modified nucleobases.)

[0745] In some embodiments, the mRNA comprises pseudouridine (y). In some embodiments, the mRNA comprises pseudouridine (y) and 5-methyl-cytidine (m5C). In some embodiments, the mRNA comprises 1 -methyl -pseudouridine (mly). In some embodiments, the mRNA comprises 1 -methyl -pseudouridine (m h| / ) and 5-methyl-cytidine (m5C). In some embodiments, the mRNA comprises 2-thiouridine (s2U). In some embodiments, the mRNA comprises 2-thiouridine and 5-methyl-cytidine (m5C). In some embodiments, the mRNA comprises 5-methoxy-uridine (mo5U). In some embodiments, the mRNA comprises 5- methoxy-uridine (mo5U) and 5-methyl-cytidine (m5C). In some embodiments, the mRNA comprises 2’-O-methyl uridine. In some embodiments, the mRNA comprises 2’-O-methyl uridine and 5-methyl-cytidine (m5C). In some embodiments, the mRNA comprises comprises N6-methyl-adenosine (m6A). In some embodiments, the mRNA comprises N6-methyl- adenosine (m6A) and 5-methyl-cytidine (m5C).

[0746] In certain embodiments, an mRNA of the disclosure is uniformly modified (i.e., fully modified, modified through-out the entire sequence) for a particular modification. For example, an mRNA can be uniformly modified with N1 -methylpseudouridine (m h| / ) or 5-methyl-cytidine (m5C), meaning that all uridines or all cytosine nucleosides in the mRNA sequence are replaced with N1 -methylpseudouridine (m h| / ) or 5-methyl-cytidine (m5C). Similarly, mRNAs of the disclosure can be uniformly modified for any type of nucleoside residue present in the sequence by replacement with a modified residue such as those set forth above.

[0747] In some embodiments, an mRNA of the disclosure may be modified in a coding region (e.g., an open reading frame encoding a polypeptide). In other embodiments, an mRNA may be modified in regions besides a coding region. For example, in some embodiments, a 5'-UTR and / or a 3'-UTR are provided, wherein either or both may independently contain one or more different nucleoside modifications. In such embodiments, nucleoside modifications may also be present in the coding region.

[0748] The mmRNAs of the disclosure can include a combination of modifications to the sugar, the nucleobase, and / or the internucleoside linkage. These combinations can include any one or more modifications described herein.

[0749] Where a single modification is listed, the listed nucleoside or nucleotide represents 100 percent of that A, U, G or C nucleotide or nucleoside having been modified. Where percentages are listed, these represent the percentage of that particular A, U, G or C nucleobase triphosphate of the total amount of A, U, G, or C triphosphate present. For example, the combination: 25 % 5-Aminoallyl-CTP + 75 % CTP / 25 % 5-Methoxy-UTP + 75 % UTP refers to a polynucleotide where 25% of the cytosine triphosphates are 5-Aminoallyl-CTP while 75% of the cytosines are CTP; whereas 25% of the uracils are 5-methoxy UTP while 75% of the uracils are UTP. Where no modified UTP is listed then the naturally occurring ATP, UTP, GTP and / or CTP is used at 100% of the sites of those nucleotides found in the polynucleotide. In this example all of the GTP and ATP nucleotides are left unmodified.

[0750] The mRNAs of the present disclosure, or regions thereof, may be codon optimized. Codon optimization methods are known in the art and may be useful for a variety of purposes: matching codon frequencies in host organisms to ensure proper folding, bias GC content to increase mRNA stability or reduce secondary structures, minimize tandem repeat codons or base runs that may impair gene construction or expression, customize transcriptional and translational control regions, insert or remove proteins trafficking sequences, remove / add post translation modification sites in encoded proteins (e.g., glycosylation sites), add, remove or shuffle protein domains, insert or delete restriction sites, modify ribosome binding sites and mRNA degradation sites, adjust translation rates to allow the various domains of the protein to fold properly, or to reduce or eliminate problem secondary structures within the polynucleotide.Codon optimization tools, algorithms and services are known in the art; non-limiting examples include services from GeneArt (Life Technologies), DNA2.0 (Menlo Park, CA) and / or proprietary methods. In some embodiments, the mRNA sequence is optimized using optimization algorithms, e.g., to optimize expression in mammalian cells or enhance mRNA stability.

[0751] In certain embodiments, the present disclosure includes polynucleotides having at least 80%, at least 85%, at least 90%, at least 95%, at least 98%, or at least 99% sequence identity to any of the polynucleotide sequences described herein.

[0752] mRNAs of the present disclosure may be produced by means available in the art, including but not limited to in vitro transcription (IVT) and synthetic methods. Enzymatic (IVT), solid-phase, liquid-phase, combined synthetic methods, small region synthesis, and ligation methods may be utilized. In some embodiments, mRNAs are made using IVT enzymatic synthesis methods. Accordingly, the present disclosure also includes polynucleotides, e.g., DNA, constructs and vectors that may be used to in vitro transcribe an mRNA described herein.

[0753] Non-natural modified nucleobases may be introduced into polynucleotides, e.g., mRNA, during synthesis or post-synthesis. In certain embodiments, modifications may be on intemucleoside linkages, purine or pyrimidine bases, or sugar. In particular embodiments, the modification may be introduced at the terminal of a polynucleotide chain or anywhere else in the polynucleotide chain; with chemical synthesis or with a polymerase enzyme.

[0754] Either enzymatic or chemical ligation methods may be used to conjugate polynucleotides or their regions with different functional moi eties, such as targeting or delivery agents, fluorescent labels, liquids, nanoparticles, etc. Therapeutic Agents for Reducing Protein Expression

[0755] In some embodiments, the therapeutic agent is a therapeutic agent that reduces (i.e., decreases, inhibits, downregulates) protein expression. Non-limiting examples of types of therapeutic agents that can be used for reducing protein expression include mRNAs that incorporate a micro-RNA binding site(s) (miR binding site), microRNAs (miRNAs), antagomirs, small (short) interfering RNAs (siRNAs) (including shortmers and dicer-substrate RNAs), RNA interference (RNAi) molecules, antisense RNAs, ribozymes, small hairpin RNAs (shRNAs), locked nucleic acids (LNAs) and CRISPR / Cas9 technology.Sensor Sequences andMicroRNA (miRNA) Binding Sites

[0756] Sensor sequences include, for example, microRNA (miRNA) binding sites, transcription factor binding sites, structured mRNA sequences and / or motifs, artificial binding sites engineered to act as pseudo-receptors for endogenous nucleic acid binding molecules, and combinations thereof. Non-limiting examples of sensor sequences are described in U.S. Publication 2014 / 0200261, the contents of which are incorporated herein by reference in their entirety.

[0757] In some embodiments, a polyribonucleotide (e.g., a ribonucleic acid (RNA), e.g., a messenger RNA (mRNA)) of the disclosure comprising an open reading frame (ORF) encoding a polypeptide further comprises a sensor sequence. In some embodiments, the sensor sequence is a miRNA binding site.

[0758] A miRNA is a 19-25 nucleotide long noncoding RNA that binds to a polyribonucleotide and down-regulates gene expression either by reducing stability or by inhibiting translation of the polyribonucleotide. A miRNA sequence comprises a “seed” region, i.e., a sequence in the region of positions 2-8 of the mature miRNA. A miRNA seed can comprise positions 2-8 or 2-7 of the mature miRNA. In some embodiments, a miRNA seed can comprise 7 nucleotides (e.g., nucleotides 2-8 of the mature miRNA), wherein the seed-complementary site in the corresponding miRNA binding site is flanked by an adenosine (A) opposed to miRNA position 1. In some embodiments, a miRNA seed can comprise 6 nucleotides (e.g., nucleotides 2-7 of the mature miRNA), wherein the seed-complementary site in the corresponding miRNA binding site is flanked by an adenosine (A) opposed to miRNA position 1. See, for example, Grimson A, Farh KK, Johnston WK, Garrett-Engel e P, Lim LP, Bartel DP; Mol Cell. 2007 Jul 6;27(1 ): 91 - 105. miRNA profiling of the target cells or tissues can be conducted to determine the presence or absence of miRNA in the cells or tissues. In some embodiments, a polyribonucleotide (e.g., a ribonucleic acid (RNA), e.g., a messenger RNA (mRNA)) of the disclosure comprises one or more microRNA target sequences, microRNA sequences, or microRNA seeds. Such sequences can correspond to any known microRNA such as those taught in US Publication US2005 / 0261218 and US Publication US2005 / 0059005, the contents of each of which are incorporated herein by reference in their entirety.

[0759] As used herein, the term “microRNA (miRNA or miR) binding site” refers to a sequence within a polyribonucleotide, e.g., within a DNA or within an RNA transcript, including in the 5'UTR and / or 3'UTR, that has sufficient complementarity to all or a region of a miRNA to interact with, associate with or bind to the miRNA. In some embodiments, a polyribonucleotide of the disclosure comprising an ORF encoding a polypeptide further comprises a miRNA binding site. In exemplary embodiments, a 5UTR and / or 3UTR of thepolyribonucleotide (e.g., a ribonucleic acid (RNA), e.g., a messenger RNA (mRNA)) comprises a miRNA binding site.

[0760] A miRNA binding site having sufficient complementarity to a miRNA refers to a degree of complementarity sufficient to facilitate miRNA-mediated regulation of a polyribonucleotide, e.g., miRNA-mediated translational repression or degradation of the polyribonucleotide. In exemplary aspects of the disclosure, a miRNA binding site having sufficient complementarity to the miRNA refers to a degree of complementarity sufficient to facilitate miRNA-mediated degradation of the polyribonucleotide, e.g., miRNA-guided RNA- induced silencing complex (RlSC)-mediated cleavage of mRNA. The miRNA binding site can have complementarity to, for example, a 19-25 nucleotide miRNA sequence, to a 19-23 nucleotide miRNA sequence, or to a 22 nucleotide miRNA sequence. A miRNA binding site can be complementary to only a portion of a miRNA, e.g., to a portion less than 1, 2, 3, or 4 nucleotides of the full length of a naturally-occurring miRNA sequence. In some embodiments, the desired regulation is mRNA degradation. In some embodiments, the miRNA binding site has full or complete complementarity (e.g., full complementarity or complete complementarity over all or a significant portion of the length of a naturally-occurring miRNA). In some embodiments, the mRNA degradation has full or complete complementarity.

[0761] In some embodiments, a miRNA binding site includes a sequence that has complementarity (e.g., partial or complete complementarity) with an miRNA seed sequence. In some embodiments, the miRNA binding site includes a sequence that has complete complementarity with a miRNA seed sequence. In some embodiments, a miRNA binding site includes a sequence that has complementarity (e.g., partial or complete complementarity) with an miRNA sequence. In some embodiments, the miRNA binding site includes a sequence that has complete complementarity with a miRNA sequence. In some embodiments, a miRNA binding site has complete complementarity with a miRNA sequence but for 1, 2, or 3 nucleotide substitutions, terminal additions, and / or truncations.

[0762] In some embodiments, the miRNA binding site is the same length as the corresponding miRNA. In some embodiments, the miRNA binding site is one, two, three, four, five, six, seven, eight, nine, ten, eleven or twelve nucleotide(s) shorter than the corresponding miRNA at the 5' terminus, the 3' terminus, or both. In still other embodiments, the microRNA binding site is two nucleotides shorter than the corresponding microRNA at the 5' terminus, the 3' terminus, or both. The miRNA binding sites that are shorter than the corresponding miRNAs are still capable of degrading the mRNA incorporating one or more of the miRNA binding sites or preventing the mRNA from translation.

[0763] In some embodiments, the miRNA binding site binds to the corresponding mature miRNA that is part of an active RISC containing Dicer. In another embodiment, binding of the miRNA binding site to the corresponding miRNA in RISC degrades the mRNA containing the miRNA binding site or prevents the mRNA from being translated. In some embodiments, the miRNA binding site has sufficient complementarity to miRNA so that a RISC complex comprising the miRNA cleaves the polyribonucleotide comprising the miRNA binding site. In some embodiments, the miRNA binding site has imperfect complementarity so that a RISC complex comprising the miRNA induces instability in the polyribonucleotide comprising the miRNA binding site. In another embodiment, the miRNA binding site has imperfect complementarity so that a RISC complex comprising the miRNA represses transcription of the polyribonucleotide comprising the miRNA binding site.

[0764] In some embodiments, the miRNA binding site has one, two, three, four, five, six, seven, eight, nine, ten, eleven or twelve mismatch(es) from the corresponding miRNA.

[0765] In some embodiments, the miRNA binding site has at least about ten, at least about eleven, at least about twelve, at least about thirteen, at least about fourteen, at least about fifteen, at least about sixteen, at least about seventeen, at least about eighteen, at least about nineteen, at least about twenty, or at least about twenty-one contiguous nucleotides complementary to at least about ten, at least about eleven, at least about twelve, at least about thirteen, at least about fourteen, at least about fifteen, at least about sixteen, at least about seventeen, at least about eighteen, at least about nineteen, at least about twenty, or at least about twenty-one, respectively, contiguous nucleotides of the corresponding miRNA.

[0766] By engineering one or more miRNA binding sites into a polyribonucleotide of the disclosure, the polyribonucleotide can be targeted for degradation or reduced translation, provided the miRNA in question is available. This can reduce off-target effects upon delivery of the polyribonucleotide. In some embodiments, if a polyribonucleotide of the disclosure is not intended to be delivered to a tissue or cell but ends up there, then a miRNA abundant in the tissue or cell can inhibit the expression of the gene of interest if one or multiple binding sites of the miRNA are engineered into the 5'UTR and / or 3'UTR of the polyribonucleotide.

[0767] Conversely, miRNA binding sites can be removed from polyribonucleotide sequences in which they naturally occur in order to increase protein expression in specific tissues. In some embodiments, a binding site for a specific miRNA can be removed from a polyribonucleotide to improve protein expression in tissues or cells containing the miRNA.

[0768] In one embodiment, a polyribonucleotide of the disclosure can include at least one miRNA-binding site in the 5'UTR and / or 3'UTR in order to direct cytotoxic or cytoprotectivemRNA therapeutics to specific cells such as, but not limited to, normal and / or cancerous cells. In another embodiment, a polyribonucleotide of the disclosure can include two, three, four, five, six, seven, eight, nine, ten, or more miRNA-binding sites in the 5'-UTR and / or 3 '-UTR in order to direct cytotoxic or cytoprotective mRNA therapeutics to specific cells such as, but not limited to, normal and / or cancerous cells.

[0769] Regulation of expression in multiple tissues can be accomplished through introduction or removal of one or more miRNA binding sites. The decision whether to remove or insert a miRNA binding site can be made based on miRNA expression patterns and / or their profilings in diseases. Identification of miRNAs, miRNA binding sites, and their expression patterns and role in biology have been reported (e.g., Bonauer et al., Curr Drug Targets 2010 11 :943-949; Anand and Cheresh Curr Opin Hematol 2011 18: 171-176; Contreras and Rao Leukemia 2012 26:404-413 (2011 Dec 20. doi: 10.1038 / leu.2011.356); Bartel Cell 2009 136:215-233; Landgraf et al, Cell, 2007 129: 1401-1414; Gentner andNaldini, Tissue Antigens. 2012 80:393- 403 and all references therein; each of which is incorporated herein by reference in its entirety).

[0770] miRNAs and miRNA binding sites can correspond to any known sequence, including non-limiting examples described in U.S. Publication Nos. 2014 / 0200261, 2005 / 0261218, and 2005 / 0059005, each of which are incorporated herein by reference in their entirety.

[0771] Examples of tissues where miRNA are known to regulate mRNA, and thereby protein expression, include, but are not limited to, liver (miR-122), muscle (miR-133, miR-206, miR- 208), endothelial cells (miR-17-92, miR-126), myeloid cells (miR-142-3p, miR-142-5p, miR- 16, miR-21, miR-223, miR-24, miR-27), adipose tissue (let-7, miR-30c), heart (miR-ld, miR- 149), kidney (miR-192, miR-194, miR-204), and lung epithelial cells (let-7, miR-133, miR- 126).

[0772] Specifically, miRNAs are known to be differentially expressed in immune cells (also called hematopoietic cells), such as antigen presenting cells (APCs) (e.g., dendritic cells and macrophages), macrophages, monocytes, B lymphocytes, T lymphocytes, granulocytes, natural killer cells, etc. Immune cell specific miRNAs are involved in immunogenicity, autoimmunity, the immune-response to infection, inflammation, as well as unwanted immune response after gene therapy and tissue / organ transplantation. Immune cells specific miRNAs also regulate many aspects of development, proliferation, differentiation and apoptosis of hematopoietic cells (immune cells). In some embodiments, miR-142 and miR-146 are exclusively expressed in immune cells, particularly abundant in myeloid dendritic cells. It has been demonstrated that the immune response to a polyribonucleotide can be shut-off by adding miR-142 binding sites to the 3'-UTR of the polyribonucleotide, enabling more stable gene transfer in tissues andcells. miR-142 efficiently degrades exogenous polyribonucleotides in antigen presenting cells and suppresses cytotoxic elimination of transduced cells (e.g., Annoni A et al., blood, 2009, 114, 5152-5161; Brown BD, et al., Nat med. 2006, 12(5), 585-591; Brown BD, et al., blood, 2007, 110(13): 4144-4152, each of which is incorporated herein by reference in its entirety).

[0773] An antigen-mediated immune response can refer to an immune response triggered by foreign antigens, which, when entering an organism, are processed by the antigen presenting cells and displayed on the surface of the antigen presenting cells. T cells can recognize the presented antigen and induce a cytotoxic elimination of cells that express the antigen.

[0774] Introducing a miR-142 binding site into the 5'UTR and / or 3'UTR of a polyribonucleotide of the disclosure can selectively repress gene expression in antigen presenting cells through miR-142 mediated degradation, limiting antigen presentation in antigen presenting cells (e.g., dendritic cells) and thereby preventing antigen-mediated immune response after the delivery of the polyribonucleotide. The polyribonucleotide is then stably expressed in target tissues or cells without triggering cytotoxic elimination.

[0775] In one embodiment, binding sites for miRNAs that are known to be expressed in immune cells, in particular, antigen presenting cells, can be engineered into a polyribonucleotide of the disclosure to suppress the expression of the polyribonucleotide in antigen presenting cells through miRNA mediated RNA degradation, subduing the antigen- mediated immune response. Expression of the polyribonucleotide is maintained in non- immune cells where the immune cell specific miRNAs are not expressed. In some embodiments, in some embodiments, to prevent an immunogenic reaction against a liver specific protein, any miR-122 binding site can be removed and a miR-142 (and / or mirR-146) binding site can be engineered into the 5'UTR and / or 3'UTR of a polyribonucleotide of the disclosure.

[0776] To further drive the selective degradation and suppression in APCs and macrophage, a polyribonucleotide of the disclosure can include a further negative regulatory element in the 5'UTR and / or 3'UTR, either alone or in combination with miR-142 and / or miR-146 binding sites. As a non-limiting example, the further negative regulatory element is a Constitutive Decay Element (CDE).

[0777] Immune cell specific miRNAs include, but are not limited to, hsa-let-7a-2-3p, hsa-let- 7a-3p, hsa-7a-5p, hsa-let-7c, hsa-let-7e-3p, hsa-let-7e-5p, hsa-let-7g-3p, hsa-let-7g-5p, hsa- let-7i-3p, hsa-let-7i-5p, miR-10a-3p, miR-10a-5p, miR-1184, hsa-let-7f-l--3p, hsa-let-7f-2— 5p, hsa-let-7f-5p, miR-125b-l-3p, miR-125b-2-3p, miR-125b-5p, miR-1279, miR-130a-3p, miR-130a-5p, miR-132-3p, miR-132-5p, miR-142-3p, miR-142-5p, miR-143-3p, miR-143-5p,miR-146a-3p, miR-146a-5p, miR-146b-3p, miR-146b-5p, miR-147a, miR-147b, miR-148a- 5p, miR-148a-3p, miR-150-3p, miR-150-5p, miR-151b, miR-155-3p, miR-155-5p, miR-15a- 3p, miR-15a-5p, miR-15b-5p, miR-15b-3p, miR-16-l-3p, miR-16-2-3p, miR-16-5p, miR-17- 5p, miR-181a-3p, miR-181a-5p, miR-18 la-2-3 p, miR-182-3p, miR-182-5p, miR-197-3p, miR-197-5p, miR-21-5p, miR-21-3p, miR-214-3p, miR-214-5p, miR-223-3p, miR-223-5p, miR-221-3p, miR-221-5p, miR-23b-3p, miR-23b-5p, miR-24-l-5p,miR-24-2-5p, miR-24-3p, miR-26a-l-3p, miR-26a-2-3p, miR-26a-5p, miR-26b-3p, miR-26b-5p, miR-27a-3p, miR-27a- 5p, miR-27b-3p,miR-27b-5p, miR-28-3p, miR-28-5p, miR-2909, miR-29a-3p, miR-29a-5p, miR-29b-l-5p, miR-29b-2-5p, miR-29c-3p, miR-29c-5p„ miR-30e-3p, miR-30e-5p, miR-331- 5p, miR-339-3p, miR-339-5p, miR-345-3p, miR-345-5p, miR-346, miR-34a-3p, miR-34a-5p, , miR-363-3p, miR-363-5p, miR-372, miR-377-3p, miR-377-5p, miR-493-3p, miR-493-5p, miR-542, miR-548b-5p, miR548c-5p, miR-548i, miR-548j, miR-548n, miR-574-3p, miR-598, miR-718, miR-935, miR-99a-3p, miR-99a-5p, miR-99b-3p, and miR-99b-5p. Furthermore, novel miRNAs can be identified in immune cell through micro-array hybridization and microtome analysis (e.g., Jima DD et al, Blood, 2010, 116:el l8-el27; Vaz C et al., BMC Genomics, 2010, 11,288, the content of each of which is incorporated herein by reference in its entirety.)

[0778] miRNAs that are known to be expressed in the liver include, but are not limited to, miR- 107, miR-122-3p, miR-122-5p, miR-1228-3p, miR-1228-5p, miR-1249, miR-129-5p, miR- 1303, miR-151a-3p, miR-151a-5p, miR-152, miR-194-3p, miR-194-5p, miR-199a-3p, miR- 199a-5p, miR-199b-3p, miR-199b-5p, miR-296-5p, miR-557, miR-581, miR-939-3p, and miR-939-5p. miRNA binding sites from any liver specific miRNA can be introduced to or removed from a polyribonucleotide of the disclosure to regulate expression of the polyribonucleotide in the liver. Liver specific miRNA binding sites can be engineered alone or further in combination with immune cell (e.g., APC) miRNA binding sites in a polyribonucleotide of the disclosure.

[0779] miRNAs that are known to be expressed in the lung include, but are not limited to, let- 7a-2-3p, let-7a-3p, let-7a-5p, miR-126-3p, miR-126-5p, miR-127-3p, miR-127-5p, miR-130a- 3p, miR-130a-5p, miR-130b-3p, miR-130b-5p, miR-133a, miR-133b, miR-134, miR-18a-3p, miR-18a-5p, miR-18b-3p, miR-18b-5p, miR-24-l-5p, miR-24-2-5p, miR-24-3p, miR-296-3p, miR-296-5p, miR-32-3p, miR-337-3p, miR-337-5p, miR-381-3p, and miR-381-5p. MiRNA binding sites from any lung specific miRNA can be introduced to or removed from a polyribonucleotide of the disclosure to regulate expression of the polyribonucleotide in thelung. Lung specific miRNA binding sites can be engineered alone or further in combination with immune cell (e.g., APC) miRNA binding sites in a polyribonucleotide of the disclosure.

[0780] miRNAs that are known to be expressed in the heart include, but are not limited to, miR-1, miR-133a, miR-133b, miR-149-3p, miR-149-5p, miR-186-3p, miR-186-5p, miR-208a, miR-208b, miR-210, miR-296-3p, miR-320, miR-451a, miR-451b, miR-499a-3p, miR-499a- 5p, miR-499b-3p, miR-499b-5p, miR-744-3p, miR-744-5p, miR-92b-3p, and miR-92b-5p. MiRNA binding sites from any heart specific microRNA can be introduced to or removed from a polyribonucleotide of the disclosure to regulate expression of the polyribonucleotide in the heart. Heart specific miRNA binding sites can be engineered alone or further in combination with immune cell (e.g., APC) miRNA binding sites in a polyribonucleotide of the disclosure.

[0781] miRNAs that are known to be expressed in the nervous system include, but are not limited to, miR-124-5p, miR-125a-3p, miR-125a-5p, miR-125b-l-3p, miR-125b-2-3p, miR- 125b-5p,miR-1271-3p, miR-1271-5p, miR-128, miR-132-5p, miR-135a-3p, miR-135a-5p, miR-135b-3p, miR-135b-5p, miR-137, miR-139-5p, miR-139-3p, miR-149-3p, miR-149-5p, miR-153, miR-181c-3p, miR-181c-5p, miR-183-3p, miR-183-5p, miR-190a, miR-190b, miR- 212-3p, miR-212-5p, miR-219-l-3p, miR-219-2-3p, miR-23a-3p, miR-23a-5p,miR-30a-5p, miR-30b-3p, miR-30b-5p, miR-30c-l-3p, miR-30c-2-3p, miR-30c-5p, miR-30d-3p, miR-30d- 5p, miR-329, miR-342-3p, miR-3665, miR-3666, miR-380-3p, miR-380-5p, miR-383, miR- 410, miR-425-3p, miR-425-5p, miR-454-3p, miR-454-5p, miR-483, miR-510, miR-516a-3p, miR-548b-5p, miR-548c-5p, miR-571, miR-7-l-3p, miR-7-2-3p, miR-7-5p, miR-802, miR- 922, miR-9-3p, and miR-9-5p. MiRNAs enriched in the nervous system further include those specifically expressed in neurons, including, but not limited to, miR-132-3p, miR-132-3p, miR- 148b-3p, miR-148b-5p, miR-151a-3p, miR-151a-5p, miR-212-3p, miR-212-5p, miR-320b, miR-320e, miR-323a-3p, miR-323a-5p, miR-324-5p, miR-325, miR-326, miR-328, miR-922 and those specifically expressed in glial cells, including, but not limited to, miR-1250, miR- 219-1 -3p, miR-219-2-3p, miR-219-5p, miR-23a-3p, miR-23a-5p, miR-3065-3p, miR-3065-5p, miR-30e-3p, miR-30e-5p, miR-32-5p, miR-338-5p, and miR-657. MiRNA binding sites from any CNS specific miRNA can be introduced to or removed from a polyribonucleotide of the disclosure to regulate expression of the polyribonucleotide in the nervous system. Nervous system specific miRNA binding sites can be engineered alone or further in combination with immune cell (e.g., APC) miRNA binding sites in a polyribonucleotide of the disclosure.

[0782] miRNAs that are known to be expressed in the pancreas include, but are not limited to, miR-105-3p, miR-105-5p, miR-184, miR-195-3p, miR-195-5p, miR-196a-3p, miR-196a-5p, miR-214-3p, miR-214-5p, miR-216a-3p, miR-216a-5p, miR-30a-3p, miR-33a-3p, miR-33a-5p, miR-375, miR-7-l-3p, miR-7-2-3p, miR-493-3p, miR-493-5p, and miR-944. MiRNA binding sites from any pancreas specific miRNA can be introduced to or removed from a polyribonucleotide of the disclosure to regulate expression of the polyribonucleotide in the pancreas. Pancreas specific miRNA binding sites can be engineered alone or further in combination with immune cell (e.g., APC) miRNA binding sites in a polyribonucleotide of the disclosure.

[0783] miRNAs that are known to be expressed in the kidney include, but are not limited to, miR-122-3p, miR-145-5p, miR-17-5p, miR-192-3p, miR-192-5p, miR-194-3p, miR-194-5p, miR-20a-3p, miR-20a-5p, miR-204-3p, miR-204-5p, miR-210, miR-216a-3p, miR-216a-5p, miR-296-3p, miR-30a-3p, miR-30a-5p, miR-30b-3p, miR-30b-5p, miR-30c-l-3p, miR-30c-2- 3p, miR30c-5p, miR-324-3p, miR-335-3p, miR-335-5p, miR-363-3p, miR-363-5p, and miR- 562. MiRNA binding sites from any kidney specific miRNA can be introduced to or removed from a polyribonucleotide of the disclosure to regulate expression of the polyribonucleotide in the kidney. Kidney specific miRNA binding sites can be engineered alone or further in combination with immune cell (e.g., APC) miRNA binding sites in a polyribonucleotide of the disclosure.

[0784] miRNAs that are known to be expressed in the muscle include, but are not limited to, let-7g-3p, let-7g-5p, miR-1, miR-1286, miR-133a, miR-133b, miR-140-3p, miR-143-3p, miR- 143-5p, miR-145-3p, miR-145-5p, miR-188-3p, miR-188-5p, miR-206, miR-208a, miR-208b, miR-25-3p, and miR-25-5p. MiRNA binding sites from any muscle specific miRNA can be introduced to or removed from a polyribonucleotide of the disclosure to regulate expression of the polyribonucleotide in the muscle. Muscle specific miRNA binding sites can be engineered alone or further in combination with immune cell (e.g., APC) miRNA binding sites in a polyribonucleotide of the disclosure.

[0785] miRNAs are also differentially expressed in different types of cells, such as, but not limited to, endothelial cells, epithelial cells, and adipocytes.

[0786] miRNAs that are known to be expressed in endothelial cells include, but are not limited to, let-7b-3p, let-7b-5p, miR-100-3p, miR-100-5p, miR-101-3p, miR-101-5p, miR-126-3p, miR-126-5p, miR-1236-3p, miR-1236-5p, miR-130a-3p, miR-130a-5p, miR-17-5p, miR-17- 3p, miR-18a-3p, miR-18a-5p, miR-19a-3p, miR-19a-5p, miR-19b-l-5p, miR-19b-2-5p, miR- 19b-3p, miR-20a-3p, miR-20a-5p, miR-217, miR-210, miR-21-3p, miR-21-5p, miR-221-3p, miR-221-5p, miR-222-3p, miR-222-5p, miR-23a-3p, miR-23a-5p, miR-296-5p, miR-361-3p, miR-361-5p, miR-421, miR-424-3p, miR-424-5p, miR-513a-5p, miR-92a-l-5p, miR-92a-2- 5p, miR-92a-3p, miR-92b-3p, and miR-92b-5p. Many novel miRNAs are discovered inendothelial cells from deep-sequencing analysis (e.g., Voellenkle C et al., RNA, 2012, 18, 472- 484, herein incorporated by reference in its entirety). MiRNA binding sites from any endothelial cell specific miRNA can be introduced to or removed from a polyribonucleotide of the disclosure to regulate expression of the polyribonucleotide in the endothelial cells.

[0787] miRNAs that are known to be expressed in epithelial cells include, but are not limited to, let-7b-3p, let-7b-5p, miR-1246, miR-200a-3p, miR-200a-5p, miR-200b-3p, miR-200b-5p, miR-200c-3p, miR-200c-5p, miR-338-3p, miR-429, miR-451a, miR-451b, miR-494, miR-802 and miR-34a, miR-34b-5p, miR-34c-5p, miR-449a, miR-449b-3p, miR-449b-5p specific in respiratory ciliated epithelial cells, let-7 family, miR-133a, miR-133b, miR-126 specific in lung epithelial cells, miR-382-3p, miR-382-5p specific in renal epithelial cells, and miR-762 specific in corneal epithelial cells. MiRNA binding sites from any epithelial cell specific miRNA can be introduced to or removed from a polyribonucleotide of the disclosure to regulate expression of the polyribonucleotide in the epithelial cells.

[0788] In addition, a large group of miRNAs are enriched in embryonic stem cells, controlling stem cell self-renewal as well as the development and / or differentiation of various cell lineages, such as neural cells, cardiac, hematopoietic cells, skin cells, osteogenic cells and muscle cells (e.g., Kuppusamy KT et al., Curr. Mol Med, 2013, 13(5), 757-764; Vidigal JA and Ventura A, Semin Cancer Biol. 2012, 22(5-6), 428-436; Goff LA et al., PLoS One, 2009, 4:e7192; Morin RD et al., Genome Res,2008,18, 610-621; Yoo JK et al., Stem Cells Dev. 2012, 21(11), 2049- 2057, each of which is herein incorporated by reference in its entirety). MiRNAs abundant in embryonic stem cells include, but are not limited to, let-7a-2-3p, let-a-3p, let-7a-5p, let7d-3p, let-7d-5p, miR-103a-2-3p, miR-103a-5p, miR-106b-3p, miR-106b-5p, miR-1246, miR-1275, miR-138-l-3p, miR-138-2-3p, miR-138-5p, miR-154-3p, miR-154-5p, miR-200c-3p, miR- 200c-5p, miR-290, miR-301a-3p, miR-301a-5p, miR-302a-3p, miR-302a-5p, miR-302b-3p, miR-302b-5p, miR-302c-3p, miR-302c-5p, miR-302d-3p, miR-302d-5p, miR-302e, miR-367- 3p, miR-367-5p, miR-369-3p, miR-369-5p, miR-370, miR-371, miR-373, miR-380-5p, miR- 423-3p, miR-423-5p, miR-486-5p, miR-520c-3p, miR-548e, miR-548f, miR-548g-3p, miR- 548g-5p, miR-548i, miR-548k, miR-5481, miR-548m, miR-548n, miR-548o-3p, miR-548o-5p, miR-548p, miR-664a-3p, miR-664a-5p, miR-664b-3p, miR-664b-5p, miR-766-3p, miR-766- 5p, miR-885-3p, miR-885-5p,miR-93-3p, miR-93-5p, miR-941,miR-96-3p, miR-96-5p, miR- 99b-3p and miR-99b-5p. Many predicted novel miRNAs are discovered by deep sequencing in human embryonic stem cells (e.g., Morin RD et al., Genome Res, 2008, 18, 610-621; Goff LA et al., PLoS One, 2009, 4:e7192; Bar M et al., Stem cells, 2008, 26, 2496-2505, the content of each of which is incorporated herein by reference in its entirety).

[0789] In one embodiment, the binding sites of embryonic stem cell specific miRNAs can be included in or removed from the 3'UTR of a polyribonucleotide of the disclosure to modulate the development and / or differentiation of embryonic stem cells, to inhibit the senescence of stem cells in a degenerative condition (e.g., degenerative diseases), or to stimulate the senescence and apoptosis of stem cells in a disease condition (e.g., cancer stem cells).

[0790] Many miRNA expression studies are conducted to profile the differential expression of miRNAs in various cancer cells / tissues and other diseases. Some miRNAs are abnormally over-expressed in certain cancer cells and others are under-expressed. In some embodiments, miRNAs are differentially expressed in cancer cells (W02008 / 154098, US2013 / 0059015, US2013 / 0042333, WO2011 / 157294); cancer stem cells (US2012 / 0053224); pancreatic cancers and diseases (US2009 / 0131348, US2011 / 0171646, US2010 / 0286232, US8389210); asthma and inflammation (US8415096); prostate cancer (US2013 / 0053264); hepatocellular carcinoma (WO2012 / 151212, US2012 / 0329672, W02008 / 054828, US8252538); lung cancer cells (WO2011 / 076143, W02013 / 033640, W02009 / 070653, US2010 / 0323357); cutaneous T cell lymphoma (W02013 / 011378); colorectal cancer cells (WO2011 / 0281756, WO201 1 / 076142); cancer positive lymph nodes (W02009 / 100430, US2009 / 0263803); nasopharyngeal carcinoma (EP2112235); chronic obstructive pulmonary disease (US2012 / 0264626, US2013 / 0053263); thyroid cancer (WO2013 / 066678); ovarian cancer cells ( US2012 / 0309645, WO2011 / 095623); breast cancer cells (W02008 / 154098, W02007 / 081740, US2012 / 0214699), leukemia and lymphoma (W02008 / 073915, US2009 / 0092974, US2012 / 0316081, US2012 / 0283310, W02010 / 018563, the content of each of which is incorporated herein by reference in its entirety.)

[0791] As a non-limiting example, miRNA binding sites for miRNAs that are over-expressed in certain cancer and / or tumor cells can be removed from the 3'UTR of a polyribonucleotide of the disclosure, restoring the expression suppressed by the over-expressed miRNAs in cancer cells, thus ameliorating the corresponsive biological function, for instance, transcription stimulation and / or repression, cell cycle arrest, apoptosis and cell death. Normal cells and tissues, wherein miRNAs expression is not up-regulated, will remain unaffected.

[0792] MiRNA can also regulate complex biological processes such as angiogenesis (e.g., miR-132) (Anand and Cheresh Curr Opin Hematol 2011 18: 171-176). In the polyribonucleotides of the disclosure, miRNA binding sites that are involved in such processes can be removed or introduced, in order to tailor the expression of the polyribonucleotides to biologically relevant cell types or relevant biological processes. In this context, the polyribonucleotides of the disclosure are defined as auxotrophic polyribonucleotides.Peptide / Polypeptide Therapeutic Agents

[0793] In some embodiments, the therapeutic agent is a peptide therapeutic agent. In some embodiments the therapeutic agent is a polypeptide therapeutic agent.

[0794] In some embodiments, the peptide or polypeptide is naturally-derived, e.g., isolated from a natural source. In other embodiments, the peptide or polypeptide is a synthetic molecule, e.g., a synthetic peptide or polypeptide produced in vitro. In some embodiments, the peptide or polypeptide is a recombinant molecule. In some embodiments, the peptide or polypeptide is a chimeric molecule. In some embodiments, the peptide or polypeptide is a fusion molecule. In some embodiments, the peptide or polypeptide therapeutic agent of the composition is a naturally occurring peptide or polypeptide. In some embodiments, the peptide or polypeptide therapeutic agent of the composition is a modified version of a naturally occurring peptide or polypeptide (e.g., contains less than 3, less than 5, less than 10, less than 15, less than 20, or less than 25 amino substitutions, deletions, or additions compared to its wild type, naturally occurring peptide or polypeptide counterpart).

[0795] In some embodiments, in the loaded LNP of the disclosure, the one or more therapeutic and / or prophylactic agents is a polynucleotide or a polypeptide.Genome Editing Techniques

[0796] In some embodiments, the nucleic acid is suitable for a genome editing technique.

[0797] In some embodiments, the genome editing technique is clustered regularly interspaced short palindromic repeats (CRISPR) or transcription activator-like effector nuclease (TALEN).

[0798] In some embodiments, the nucleic acid is at least one nucleic acid suitable for a genome editing technique selected from the group consisting of a CRISPR RNA (crRNA), a transactivating crRNA (tracrRNA), a single guide RNA (sgRNA), and a DNA repair template.Vaccines

[0799] In some embodiments, the therapeutic and / or prophylactic is a ribonucleic acid (RNA) cancer vaccine of an RNA (e.g., messenger RNA (mRNA)) that can safely direct the body' s cellular machinery to produce nearly any cancer protein or fragment thereof of interest. In some embodiments, the RNA is a modified RNA. The RNA vaccines of the present disclosure may be used to induce a balanced immune response against cancers, comprising both cellular and humoral immunity, without risking the possibility of insertional mutagenesis, for example.

[0800] The RNA vaccines may be utilized in various settings depending on the prevalence of the cancer or the degree or level of unmet medical need. The RNA vaccines may be utilized to treat and / or prevent a cancer of various stages or degrees of metastasis. The RNA vaccines have superior properties in that they produce much larger antibody titers and produce responses earlier than alternative anti-cancer therapies including cancer vaccines. While not wishing to be bound by theory, it is believed that the RNA vaccines, as mRNA polynucleotides, are better designed to produce the appropriate protein conformation upon translation as the RNA vaccines co-opt natural cellular machinery. Unlike traditional vaccines which are manufactured ex vivo and may trigger unwanted cellular responses, the RNA vaccines are presented to the cellular system in a more native fashion.

[0801] Some embodiments of the present disclosure provide cancer vaccines that include at least one ribonucleic acid (RNA) polynucleotide having an open reading frame encoding at least one cancer antigenic polypeptide or an immunogenic fragment thereof {e.g., an immunogenic fragment capable of inducing an immune response to cancer). Other embodiments include at least one ribonucleic acid (RNA) polynucleotide having an open reading frame encoding two or more antigens or epitopes capable of inducing an immune response to cancer.

[0802] The invention in some aspects is a vaccine of a mRNA having an open reading frame encoding a cancer antigen and a mRNA having an open reading frame encoding an immune checkpoint modulator. In some embodiments the immune checkpoint modulator is an inhibitory checkpoint polypeptide. In some embodiments, the inhibitory checkpoint polypeptide is an antibody or fragment thereof that specifically binds to a molecule selected from the group consisting of PD-1, TIM-3, VISTA, A2AR, B7-H3, B7-H4, BTLA, CTLA-4, IDO, KIR and LAG3. The inhibitory checkpoint polypeptide is an anti-CTLA4 or anti-PDl antibody in some embodiments. Optionally the vaccine includes a lipid nanoparticle. In some embodiments a vaccine of a mRNA having an open reading frame encoding a cancer antigen is administered to a subject. In other embodiments a checkpoint inhibitor 3-10 weeks later. In some embodiments the checkpoint inhibitor is administered 4 weeks later.

[0803] In other aspects the invention is a personalized cancer vaccine of a mRNA having an open reading frame encoding at least 2 cancer antigens, wherein the at least 2 cancer antigens are patient specific cancer antigens, and a lipid nanoparticle carrier. In some embodiments the lipid nanoparticle has a mean diameter of 50-200 nm.

[0804] In yet other aspects, the invention is a personalized cancer vaccine of a mRNA having an open reading frame encoding at least 2 cancer antigens wherein the at least 2 cancer antigensare representative of antigens of a patient. In some embodiments, the antigens of a patient are exosome identified antigens of the patient. In some embodiments a single mRNA encodes the cancer antigens. In other embodiments a plurality of mRNA encode the cancer antigens.

[0805] Each mRNA may encode 5-10 cancer antigens or a single cancer antigen in other embodiments. In some embodiments the mRNA encodes 2-100 cancer antigens. In other embodiments mRNA encodes 10-100, 20-100, 50-100, 100-200, 300-400, 500-600, 600-700, 700-800, 900-1,000, or 1,000-10,000 cancer antigens.

[0806] In some embodiments, a) the mRNA encoding each cancer antigen is interspersed by cleavage sensitive sites; b) the mRNA encoding each cancer antigen is linked directly to one another without a linker ; c) the mRNA encoding each cancer antigen is linked to one another with a single nucleotide linker; d) each cancer antigen comprises a 25-35 amino acids and includes a centrally located SNP mutation; e) at least 30% of the cancer antigens have a highest affinity for class I MHC molecules from the subject; f) at least 30% of the cancer antigens have a highest affinity for class II MHC molecules from the subject; g) at least 50% of the cancer antigens have a predicted binding affinity of IC >500nM for HLA- A, HLA-B and / or DRB 1; h) the mRNA encodes 20 cancer antigens; i) 50% of the cancer antigens have a binding affinity for class I MHC and 50% of the cancer antigens have a binding affinity for class II MHC; and / or j) the mRNA encoding the cancer antigens is arranged such that the cancer antigens are ordered to minimize pseudo-epitopes.

[0807] In some embodiments, each cancer antigen comprises 31 amino acids and includes a centrally located SNP mutation with 15 flanking amino acids on each side of the SNP mutation.

[0808] In some embodiments the vaccine is a personalized cancer vaccine and wherein the cancer antigen is a subject specific cancer antigen. In some embodiments, the subject specific cancer antigen may be representative of an exome of a tumor sample of the subject, or of a transcriptome of a tumor sample of the subject. In some embodiments, the subject specific cancer antigen may be representative of an exosome of the subject.

[0809] In some embodiments, the open reading frame further encodes one or more traditional cancer antigens. In some embodiments, the traditional cancer antigen is a non-mutated antigen. In some embodiments, the traditional cancer antigen is a mutated antigen.

[0810] In some embodiments, the mRNA vaccine further comprises an mRNA having an open reading frame encoding one or more traditional cancer antigens.

[0811] In some embodiments a single mRNA encodes the cancer antigens. In other embodiments a plurality of mRNA encode the cancer antigens. Each cancer antigen is 10-50 amino acids in length in some embodiments. In other embodiments each cancer antigen is 15- 20 amino acids in length. In other embodiments the cancer antigen is 20-50, 25-100, 100-200, 200-300, 300-400, 400-500, 500-1,000, or 1,000-10,000 amino acids in length.

[0812] In some embodiments, the vaccines further comprise an adjuvant.

[0813] Some embodiments of the present disclosure provide a cancer vaccine that includes at least one ribonucleic acid (RNA) polynucleotide having an open reading frame encoding at least one cancer polypeptide, at least one 5' terminal cap and at least one chemical modification, formulated within a lipid nanoparticle. In some embodiments, a 5' terminal cap is 7mG(5')ppp(5')NlmpNp.

[0814] In some embodiments, at least one chemical modification is selected from pseudouridine, Nl-methylpseudouridine, Nl-ethylpseudouridine, 2-thiouridine, 4'- thiouridine, 5-methylcytosine, 2-thio-l -methyl- 1-deaza-pseudouridine, 2-thio-l-methyl- pseudouridine, 2- thio-5-aza-uridine , 2-thio-dihydropseudouridine, 2-thio-dihydrouridine, 2- thiopseudouridine, 4-methoxy-2-thio-pseudouridine, 4-methoxy-pseudouridine, 4-thio-l- methylpseudouridine, 4-thio-pseudouridine, 5-aza-uridine, dihydropseudouridine, 5- methyluridine, 5-methoxyuridine and 2' -O-methyl uridine. In some embodiments the extent of incorporation of chemically modified nucleotides has been optimized for improved immune responses to the vaccine formulation.

[0815] In some embodiments, a lipid nanoparticle (e.g., an empty LNP or a loaded LNP of the disclosure) comprises a cationic lipid, a PEG-modified lipid, a sterol and a non-cationic lipid. In some embodiments, a cationic lipid is an ionizable cationic lipid and the non-cationic lipid is a neutral lipid, and the sterol is a cholesterol. In some embodiments, a cationic lipid is selected from 2,2-dilinoleyl-4-dimethylaminoethyl- [l,3]-dioxolane (DLin-KC2-DMA), dilinoleyl-methyl-4-dimethylaminobutyrate (DLin-MC3- DMA), and di((Z)-non-2-en-l-yl) 9- ((4-(dimethylamino)butanoyl)oxy)heptadecanedioate (L319).

[0816] In some embodiments the lipid nanoparticle formulation includes an immune potentiator (e.g., TLR agonist) to enhance immunogenicity of the vaccine (formulation).

[0817] In some embodiments, 100% of the uracil in the open reading frame have a chemical modification. In some embodiments, a chemical modification is in the 5-position of the uracil. In some embodiments, a chemical modification is a Nl-methyl pseudouridine.

[0818] In other embodiments a mRNA encoding an APC reprograming molecule is included in the vaccine or coadministered with the vaccine. The APC reprograming molecule may be a CIITA, a chaperone protein such as CLIP, HLA-DO, HLA-DM, a costimulatory molecule such as CD40, CD80, CD86, a CIITA fragment such as amino acids 26-137 of CIITA or a protein having 80% sequence identity to CIITA.

[0819] In other aspects a method of eliciting an immune response in a subject by identifying at least 2 cancer antigens from a sample of a subject, wherein the at least 2 cancer antigens include mutations selected from the group consisting of frame-shift mutations and recombinations, and administering a mRNA vaccine having an open reading frame encoding the at least 2 cancer antigens to the subject is provided.

[0820] In some embodiments, the cancer antigens are identified from an exosome of the subject. In some embodiments 2-100 antigens are identified from the exosome. In other embodiments the mRNA vaccine has an open reading frame encoding the 2-100 antigens. A single mRNA or a plurality of mRNA may encode the antigens.

[0821] In some embodiments the antigens are cancer antigens. The cancer antigens may have mutations selected from point mutations, frame-shift mutations and recombinations. The method may further involve confirming that the cancer antigens are subject specific by exome analysis.

[0822] In some embodiments the method may further involve confirming that the cancer antigens are subject specific by transcriptome analysis.

[0823] In some embodiments the method also involves at least one month after the administration of the mRNA vaccine, identifying at least 2 cancer antigens from a sample of the subj ect to produce a second set of cancer antigens, and administering to the subj ect a mRNA vaccine having an open reading frame encoding the second set of cancer antigens to the subject.

[0824] In other embodiments the sample of the subject is a tumor sample.

[0825] In other aspects the invention comprises a method of eliciting an immune response in a subject by identifying at least 2 cancer antigens from a sample of a subject to produce a first set of cancer antigens, administering to the subject a mRNA vaccine having an open reading frame encoding the first set of cancer antigens to the subject, at least one month after the administration of the mRNA vaccine, identifying at least 2 cancer antigens from a sample of asubject to produce a second set of cancer antigens, and administering to the subject a mRNA vaccine having an open reading frame encoding the second set of cancer antigens to the subject.

[0826] The mRNA vaccine having an open reading frame encoding second set of antigens, in some embodiments, is administered to the subject 6 months to 1 year after the mRNA vaccine having an open reading frame encoding first set of cancer antigens. In other embodiments the mRNA vaccine having an open reading frame encoding second set of antigens is administered to the subject 1-2 years after the mRNA vaccine having an open reading frame encoding first set of cancer antigens.

[0827] In some embodiments a single mRNA has an open reading frame encoding the cancer antigens. In other embodiments a plurality of mRNA encode the antigens. In some embodiments the second set of cancer antigens includes 2-100 antigens. In other embodiments the cancer antigens have mutations selected from point mutations, frame-shift mutations and recombinations.

[0828] In other aspects the invention comprises a method of eliciting an immune response in a subject, by identifying at least 2 cancer antigens from a sample of a subject, administering a mRNA having an open reading frame encoding the at least 2 cancer antigens to the subject, and administering a cancer therapeutic agent to the subject. In some embodiments the cancer therapeutic agent is a targeted therapy. The targeted therapy may be a BRAF inhibitor such as vemurafenib (PLX4032) or dabrafenib.

[0829] In other embodiments the cancer therapeutic agent is a T-cell therapeutic agent. The T- cell therapeutic agent may be a checkpoint inhibitor such as an anti-PD- 1 antibody or an anti- CTLA-4 antibody. In some embodiments the anti-PD- 1 antibody is BMS-936558 (nivolumab). In other embodiments the anti-CTLA-4 antibody is ipilimumab. The T-cell therapeutic agent in other embodiments is OX40L. In yet other embodiments the cancer therapeutic agent is a vaccine comprising a population based tumor specific antigen.

[0830] In other embodiments the cancer therapeutic agent is a vaccine comprising an mRNA having an open reading frame encoding one or more traditional cancer antigens.

[0831] In some embodiments, the mRNA having an open reading frame encoding the at least 2 cancer antigens is administered to the subject simultaneously with the cancer therapeutic agent. In some embodiments, the mRNA having an open reading frame encoding the at least 2 cancer antigens is administered to the subject before administration of the cancer therapeutic agent. In some embodiments, the mRNA having an open reading frame encoding the at least 2 cancer antigens is administered to the subject after administration of the cancer therapeutic agent.

[0832] A method comprising mixing a mRNA having an open reading frame encoding a cancer antigen with a lipid nanoparticle formulation to produce a mRNA cancer vaccine, and administering the mRNA cancer vaccine to a subject within 24 hours of mixing is provided in other aspects of the invention. In some embodiments the mRNA cancer vaccine is administered to the subject within 12 hours of mixing. In other embodiments the mRNA cancer vaccine is administered to the subject within 1 hour of mixing. The mRNA cancer vaccine encodes 2-100 cancer antigens or 10-100 cancer antigens in some embodiments.

[0833] In some embodiments the vaccine is a personalized cancer vaccine and wherein the cancer antigen is a subject specific cancer antigen.

[0834] In some embodiments a single mRNA encodes the cancer antigens. In other embodiments a plurality of mRNA encode the cancer antigens. Each mRNA encodes 5-10 cancer antigens or a single cancer antigen in other embodiments. In yet other embodiments each cancer antigen is 10-50 amino acids in length or 15-20 amino acids in length.

[0835] Further provided herein are uses of cancer vaccines in the manufacture of a medicament for use in a method of inducing an antigen specific immune response in a subject, the method comprising administering the cancer vaccine to the subject in an amount effective to produce an antigen specific immune response.

[0836] A method of treating cancer in a subject in need thereof by identifying at least 2 cancer antigens from an exosome isolated from the subject; producing, based on the identified antigens, a mRNA vaccine having an open reading frame encoding the antigens; and administering the mRNA vaccine to the subject, wherein the mRNA vaccine induces a tumorspecific immune response in the subject, thereby treating cancer in the subject is provided in other aspects. The invention in other aspects is a RNA vaccine preparable according to a method involving identifying at least 2 cancer antigens from an exosome isolated from a subject; producing, based on the identified antigens, a mRNA vaccine having an open reading frame encoding the antigens.

[0837] A method of eliciting an immune response in a subject against a cancer antigen is provided in aspects of the invention. The method involves administering to the subject a RNA vaccine comprising at least one RNA polynucleotide having an open reading frame encoding at least one antigenic polypeptide or an immunogenic fragment thereof, thereby inducing in the subject an immune response specific to the antigenic polypeptide or an immunogenic fragment thereof, wherein the anti-antigenic polypeptide antibody titer in the subject is increased following vaccination relative to anti-antigenic polypeptide antibody titer in a subject vaccinated with a prophylactically effective dose of a traditional vaccine against the cancer.An "anti-antigenic polypeptide antibody" is a serum antibody the binds specifically to the antigenic polypeptide.

[0838] A prophylactically effective dose is a therapeutically effective dose that prevents advancement of cancer at a clinically acceptable level. In some embodiments the therapeutically effective dose is a dose listed in a package insert for the vaccine. A traditional vaccine, as used herein, refers to a vaccine other than the mRNA vaccines of the invention. For instance, a traditional vaccine includes but is not limited to live microorganism vaccines, killed microorganism vaccines, subunit vaccines, protein antigen vaccines, DNA vaccines, etc. In exemplary embodiments, a traditional vaccine is a vaccine that has achieved regulatory approval and / or is registered by a national drug regulatory body, for example the Food and Drug Administration (FDA) in the United States or the European Medicines Agency (EMA.)

[0839] In some embodiments the anti-antigenic polypeptide antibody titer in the subject is increased 1 log to 10 log following vaccination relative to anti-antigenic polypeptide antibody titer in a subject vaccinated with a prophylactically effective dose of a traditional vaccine against the cancer.

[0840] In some embodiments the anti-antigenic polypeptide antibody titer in the subject is increased 1 log following vaccination relative to anti -antigenic polypeptide antibody titer in a subject vaccinated with a prophylactically effective dose of a traditional vaccine against the cancer.

[0841] In some embodiments the anti-antigenic polypeptide antibody titer in the subject is increased 2 log following vaccination relative to anti -antigenic polypeptide antibody titer in a subject vaccinated with a prophylactically effective dose of a traditional vaccine against the cancer.

[0842] In some embodiments the anti-antigenic polypeptide antibody titer in the subject is increased 3 log following vaccination relative to anti -antigenic polypeptide antibody titer in a subject vaccinated with a prophylactically effective dose of a traditional vaccine against the cancer.

[0843] In some embodiments the anti-antigenic polypeptide antibody titer in the subject is increased 5 log following vaccination relative to anti -antigenic polypeptide antibody titer in a subject vaccinated with a prophylactically effective dose of a traditional vaccine against the or cancer.

[0844] In some embodiments the anti-antigenic polypeptide antibody titer in the subject is increased 10 log following vaccination relative to anti -antigenic polypeptide antibody titer ina subject vaccinated with a prophylactically effective dose of a traditional vaccine against the or cancer.

[0845] A method of eliciting an immune response in a subject against a cancer antigen is provided in other aspects of the invention. The method involves administering to the subject a RNA vaccine comprising at least one RNA polynucleotide having an open reading frame encoding at least one antigenic polypeptide or an immunogenic fragment thereof, thereby inducing in the subject an immune response specific to antigenic polypeptide or an immunogenic fragment thereof, wherein the immune response in the subject is equivalent to an immune response in a subject vaccinated with a traditional vaccine against the cancer antigen at 2 times to 100 times the dosage level relative to the RNA vaccine.

[0846] In some embodiments the immune response in the subject is equivalent to an immune response in a subject vaccinated with a traditional vaccine at twice the dosage level relative to the RNA vaccine.

[0847] In some embodiments the immune response in the subject is equivalent to an immune response in a subject vaccinated with a traditional vaccine at three times the dosage level relative to the RNA vaccine.

[0848] In some embodiments the immune response in the subject is equivalent to an immune response in a subject vaccinated with a traditional vaccine at 4 times the dosage level relative to the RNA vaccine.

[0849] In some embodiments the immune response in the subject is equivalent to an immune response in a subject vaccinated with a traditional vaccine at 5 times the dosage level relative to the RNA vaccine. In some embodiments the immune response in the subject is equivalent to an immune response in a subject vaccinated with a traditional vaccine at 10 times the dosage level relative to the RNA vaccine.

[0850] In some embodiments the immune response in the subject is equivalent to an immune response in a subject vaccinated with a traditional vaccine at 50 times the dosage level relative to the RNA vaccine.

[0851] In some embodiments the immune response in the subject is equivalent to an immune response in a subj ect vaccinated with a traditional vaccine at 100 times the dosage level relative to the RNA vaccine.

[0852] In some embodiments the immune response in the subject is equivalent to an immune response in a subject vaccinated with a traditional vaccine at 10 times to 1000 times the dosage level relative to the RNA vaccine.

[0853] In some embodiments the immune response in the subject is equivalent to an immune response in a subj ect vaccinated with a traditional vaccine at 100 times to 1000 times the dosage level relative to the RNA vaccine.

[0854] In other embodiments the immune response is assessed by determining antibody titer in the subject.

[0855] In other aspects the invention comprises a method of eliciting an immune response in a subject against a by administering to the subject a RNA vaccine comprising at least one RNA polynucleotide having an open reading frame encoding at least one cancer antigenic polypeptide or an immunogenic fragment thereof, thereby inducing in the subject an immune response specific to the antigenic polypeptide or an immunogenic fragment thereof, wherein the immune response in the subject is induced 2 days to 10 weeks earlier relative to an immune response induced in a subject vaccinated with a prophylactically effective dose of a traditional vaccine against the cancer antigen. In some embodiments the immune response in the subject is induced in a subject vaccinated with a prophylactically effective dose of a traditional vaccine at 2 times to 100 times the dosage level relative to the RNA vaccine.

[0856] In some embodiments the immune response in the subject is induced 2 days earlier relative to an immune response induced in a subject vaccinated with a prophylactically effective dose of a traditional vaccine.

[0857] In some embodiments the immune response in the subject is induced 3 days earlier relative to an immune response induced in a subject vaccinated a prophylactically effective dose of a traditional vaccine. In some embodiments the immune response in the subject is induced 1 week earlier relative to an immune response induced in a subject vaccinated with a prophylactically effective dose of a traditional vaccine.

[0858] In some embodiments the immune response in the subject is induced 2 weeks earlier relative to an immune response induced in a subject vaccinated with a prophylactically effective dose of a traditional vaccine.

[0859] In some embodiments the immune response in the subject is induced 3 weeks earlier relative to an immune response induced in a subject vaccinated with a prophylactically effective dose of a traditional vaccine.

[0860] In some embodiments the immune response in the subject is induced 5 weeks earlier relative to an immune response induced in a subject vaccinated with a prophylactically effective dose of a traditional vaccine.

[0861] In some embodiments the immune response in the subject is induced 10 weeks earlier relative to an immune response induced in a subject vaccinated with a prophylactically effective dose of a traditional vaccine.

[0862] A method of eliciting an immune response in a subject against an cancer by administering to the subject a cancer RNA vaccine having an open reading frame encoding a first antigenic polypeptide, wherein the RNA polynucleotide does not include a stabilization element, and wherein an adjuvant is not coformulated or co-administered with the vaccine.

[0863] In yet other aspects the invention comprises a method of producing an mRNA encoding a concatemeric cancer antigen comprising between 1000 and 3000 nucleotides, the method by(a) binding a first polynucleotide comprising an open reading frame encoding the concatemeric cancer antigen and a second polynucleotide comprising a 5'-UTR to a polynucleotide conjugated to a solid support;(b) ligating the 3 '-terminus of the second polynucleotide to the 5 '-terminus of the first polynucleotide under suitable conditions, wherein the suitable conditions comprise a DNA Ligase, thereby producing a first ligation product;(c) ligating the 5' terminus of a third polynucleotide comprising a 3'-UTR to the 3'- terminus of the first ligation product under suitable conditions, wherein the suitable conditions comprise an RNA Ligase, thereby producing a second ligation product; and(d) releasing the second ligation product from the solid support, thereby producing an mRNA encoding the concatemeric cancer antigen comprising between 1000 and 3000 nucleotides. In some embodiments of any one of the provided compositions or methods, the mRNA encodes one or more recurrent polymorphisms. In some embodiments, the one or more recurrent polymorphisms comprises a recurrent somatic cancer mutation in p53. In some such embodiments, the one or more recurrent somatic cancer mutation in p53 are selected from the group consisting of:(1) mutations at the canonical 5' splice site neighboring codon p.T125;(2) mutations at the canonical 5' splice site neighboring codon p.331 ;(3) mutations at the canonical 3' splice site neighboring codon p.126;(4) mutations at the canonical 5' splice site neighboring codon p.224, inducing a cryptic alternative intronic 5' splice site.

[0864] In one embodiment, the invention provides a cancer therapeutic vaccine comprising mRNA encoding an open reading frame (ORF) coding for one or more of neoantigen peptides (1) through (4). In one embodiment, the invention provides the selective administration of a vaccine containing or coding for one or more of peptides (l)-(4), based on the patient's tumorcontaining any of the above mutations. In one embodiment, the invention provides the selective administration of the vaccine based on the dual criteria of the subject's tumor containing any of the above mutations and the subject's normal HLA type containing the corresponding HLA allele predicted to bind to the resulting neoantigen.

[0865] A method for treating a subject with a personalized mRNA cancer vaccine, by isolating a sample from a subject, identifying a set of neoepitopes by analyzing a patient transcriptome and / or a patient exome from the sample to produce a patient specific mutanome, selecting a set of neoepitopes for the vaccine from the mutanome based on MHC binding strength, MHC binding diversity, predicted degree of immunogenicity, low self reactivity, and / or T cell reactivity, preparing the mRNA vaccine to encode the set of neoepitopes and administering the mRNA vaccine to the subject within two months of isolating the sample from the subject is provided in other aspects of the invention. In some embodiments the mRNA vaccine is administered to the subject within one month of isolating the sample from the subject.

[0866] In other aspects the invention comprises a method of identifying a set of neoepitopes for use in a personalized mRNA cancer vaccine having one or more polynucleotides that encode the set of neoepitopes by a. identifying a patient specific mutanome by analyzing a patient transcriptome and a patient exome, b. selecting a subset of 15-500 neoepitopes from the mutanome using a weighted value for the neoepitopes based on at least three of: an assessment of gene or transcript-level expression in patient RNA-seq; variant call confidence score; RNA- seq allele- specific expression; conservative vs. non-conservative amino acid substitution; position of point mutation (Centering Score for increased TCR engagement); position of point mutation (Anchoring Score for differential HLA binding); Selfness: <100% core epitope homology with patient WES data; HLA-A and -B IC50 for 8mers-l Imers; HLA-DRB 1 IC50 for 15mers-20mers; promiscuity Score (i.e. number of patient HLAs predicted to bind); HLA- C IC50 for 8mers-l lmers;HLA-DRB3-5 IC50 for 15mers-20mers; HLA-DQB 1 / A1 IC50 for 15mers-20mers; HLA-DPB 1 / A1 IC50 for 15mers-20mers; Class I vs Class II proportion; Diversity of patient HLA-A, -B and DRB 1 allotypes covered; proportion of point mutation vs complex ...

Claims

CLAIMSWHAT IS CLAIMED IS:

1. A method of preparing an empty-lipid nanoparticle solution (empty -LNP solution), wherein the method comprises: i) a nanoprecipitation step, comprising: i-a) a mixing step, comprising mixing a lipid solution comprising an ionizable lipid, a structural lipid, and a phospholipid, with a first aqueous buffer solution, thereby forming an intermediate empty-lipid nanoparticle solution (intermediate empty-LNP solution) comprising an intermediate empty lipid nanoparticle (intermediate empty LNP); i-b) a holding step, comprising holding the intermediate empty-LNP solution for a residence time; and i-c) a diluting step, comprising adding a diluting solution comprising a second aqueous buffer solution to the intermediate empty-LNP solution, thereby forming the empty-LNP solution comprising an empty LNP, wherein the lipid solution, the aqueous buffer solution, and / or the diluting solution comprises a phosphatidylserine phospholipid.

2. The method of claim 1, wherein the first aqueous buffer solution comprises a phosphatidylserine phospholipid.

3. The method of claim 1 or 2, wherein the first aqueous buffer solution has a pH value higher than the pKa value of the ionizable lipid.

4. The method of any one of claims 1-3, wherein the first aqueous buffer solution comprises phosphate.

5. The method of any one of claims 1-4, wherein the first aqueous buffer solution has a pH value of of about 11.0±3.0, about 11.0±2.0, about 11.0±1.5, about 11.0±1.0, about 11.0±0.9, about 11.0±0.8, about 11.0±0.7, about 11.0±0.6, about 11.0±0.5, about 11.0±0.4, about 11.0±0.3, about 11.0±0.2, or about 11.0±0.1 (e.g., about 11.6).

6. The method of any one of claims 1-5, wherein the mixing step is performed at a pH value of of about 11.0±3.0, about 11.0±2.0, about 11.0±1.5, about 11.0±1.0, about 11.0±0.9,about 11.0±0.8, about 11.0±0.7, about 11.0±0.6, about 11.0±0.5, about 11.0±0.4, about 11.0±0.3, about 11.0±0.2, or about 11.0±0.1 (e.g., about 11.6).

7. The method of any one of claims 1-6, wherein the empty LNP further comprises a PEG lipid.

8. The method of any one of claims 1-7, wherein the lipid solution further comprises a PEG lipid.

9. The method of any one of claims 1-7, wherein the lipid solution is free of PEG lipid.

10. The method of any one of claims 1-9, wherein the second aqueous buffer solution has a pH value lower than the pKa value of the ionizable lipid.

11. The method of any one of claims 1-10, wherein the second aqueous buffer solution is an acetate buffer.

12. The method of any one of claims 1-11, wherein the second aqueous buffer has a pH value of 5.0±2.0, 5.0±1.5, 5.0±1.0, 5.0±0.9, 5.0±0.8, 5.0±0.7, 5.0±0.6, 5.0±0.5, 5.0±0.4, 5.0±0.3, 5.0±0.2, or 5.0±0.1 (e.g., about 4.4).

13. The method of any one of claims 1-9, wherein the second aqueous buffer solution has a pH value higher than the pKa value of the ionizable lipid.

14. The method of claim 13, wherein the second aqueous buffer solution is a phosphate buffer.

15. The method of claim 13 or 14, wherein the second aqueous buffer has a pH value of 11.0±3.0, 11.0±2.0, 11.0±1.5, l l.Oil.O, 11.0±0.9, 11.0±0.8, 11.0±0.7, 11.0±0.6, 11.0±0.5, 11.0±0.4, 11.0±0.3, 11.0±0.2, or 11.0±0.1 (e.g., about 11.6).

16. The method of any one of claims 1-15, wherein the diluting solution is free of PEG lipid.

17. The method of any one of claims 1-15, wherein the diluting solution comprises a PEG lipid.

18. The method of any one of claims 1-17, wherein the method further comprises ii) processing the empty-LNP solution, thereby forming an empty-LNP formulation.

19. The method of claim 18, wherein processing the empty-LNP solution comprises buffer exchange.

20. The method of claim 19, wherein processing the empty-LNP solution further comprises adding a cryoprotectant and / or filtration.

21. The method of any one of claims 18-20, wherein the empty-LNP formulation comprise acetate buffer.

22. The method of any one of claims 18-21, wherein the empty-LNP formulation has a pH of 5.0±2.0, 5.0±1.5, 5.0±1.0, 5.0±0.9, 5.0±0.8, 5.0±0.7, 5.0±0.6, 5.0±0.5, 5.0±0.4, 5.0±0.3, 5.0±0.2, or 5.0±0.1 (e.g., about 5.0).

23. The method of any one of claims 1-22, wherein the method further comprises iii) a loading step, comprising mixing a nucleic acid solution comprising a nucleic acid with the empty-LNP solution or empty-LNP formulation, thereby forming the loaded-LNP solution comprising a loaded lipid nanoparticle (loaded LNP).

24. The method of claim 23, wherein nucleic acid is a messenger nucleic acid (mNRA).

25. The method of claim 23 or 24, wherein the loading step is performed at a pH of 4.5±1.5, 4.5±1.4, 4.5±1.3, 4.5±1.2, 4.5±1.1, 4.5±1.0, 4.5±0.9, 4.5±0.8, 4.5±0.7, 4.5±0.6, 4.5±0.5, 4.5±0.4, 4.5±0.3, 4.5±0.2, or 4.5±0.1 (e.g., about 4, 4.5 or 5).

26. The method of any one of claims 1-25, wherein the method further comprises iv) processing the loaded-LNP solution, thereby forming a loaded-LNP formulation.

27. The method of any one of claims 1-26, wherein the phosphatidylserine phospholipid is of Formula (PPSL-I):or a salt thereof, wherein: n is O, 1, 2, 3, 4, 5, 6, 7, 8, 9, or 10; m is 0, 1, 2, 3, 4, 5, 6, 7, 8, 9, or 10;A is of the formula:each instance of L2is independently a bond or an optionally substituted Ci-6 alkylene, wherein one methylene unit of the optionally substituted Ci-6 alkylene is optionally replaced with -O-, -N(RN)-, -S-, -C(O)-, -C(O)N(RN)-, -NRNC(O)-, -C(O)O-, -OC(O)-, -OC(O)O-, -OC(O)N(RN)-, -NRNC(O)O-, or -NRNC(O)N(RN)-; each instance of R2is independently cholesterol, optionally substituted cycloalkyl, optionally substituted C1-30 alkyl, optionally substituted C1-30 alkenyl, or optionally substitutedCi-30 alkynyl; optionally wherein one or more methylene units of the optionally substituted Cn 30 alkyl, optionally substituted C1-30 alkenyl, or optionally substituted C1-30 alkynyl are independently replaced with optionally substituted carbocyclylene, optionally substituted heterocyclylene, optionally substituted arylene, optionally substituted heteroarylene, -N(RN)-, -O-, -S-, -C(O)-, -C(O)N(RN)-, -NRNC(O)-, -NRNC(O)N(RN)-, -C(O)O-, -OC(O)-, -OC(O)O-, -OC(O)N(RN)-, -NRNC(O)O-, -C(O)S-, -SC(O)-, -C(=NRN)-, -C(=NRN)N(RN)-,-NRNC(=NRN)-, -NRNC(=NRN)N(RN)-, -C(S)-, -C(S)N(RN)-, -NRNC(S)-, -NRNC(S)N(RN)-, -S(O)-, -OS(O)-, -S(O)O-, -OS(O)O-, -OS(O)2-, -S(O)2O-, -OS(O)2O-, -N(RN)S(O)-, -S(O)N(RN)-, -N(RN)S(O)N(RN)-, -OS(O)N(RN)-, -N(RN)S(O)O-, -S(O)2-, -N(RN)S(O)2-, -S(O)2N(RN)-, -N(RN)S(O)2N(RN)-, -OS(O)2N(RN)-, or -N(RN)S(O)2O-; each instance of RNis independently hydrogen, optionally substituted alkyl, or a nitrogen protecting group;Ring B is optionally substituted carbocyclyl, optionally substituted heterocyclyl, optionally substituted aryl, or optionally substituted heteroaryl; and p is 1 or 2.

28. The method of claim 27, wherein the phosphatidylserine phospholipid is of Formula (PL-Ia):or a salt thereof.

29. The method of claim 27 or 28, wherein n is 0 and m is 1.

30. The method of any one of claims 27-29, wherein the phosphatidylserine phospholipid is of Formula (PL-Ib):or a salt thereof.

31. The method of any one of claims 27-29, wherein each instance of R2is independently Ci-30, C9-21, Cii-19, or C13-17 alkyl or C1-30, C9-21, Cn-19, or C13-17 alkenyl.

32. The method of claim 27 wherein the phosphatidylserine phospholipid isor a salt thereof.

33. An empty -LNP prepared by the method of any one of the preceding claims.

34. A method of delivering the loaded-LNP prepared by the method of any one of the preceding claims to bone marrow or spleen, comprising administering the loaded-LNP to a subject.

35. Use of the loaded-LNP prepared by the method of any one of the preceding claims in the manufacture of a medicament for delivering to bone marrow or spleen of a subject.

36. The loaded-LNP prepared by the method of any one of the preceding claims for use in delivering to bone marrow or spleen.

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